BG60913B1 - 4-бензил изоксазолови производни, метод за получаването им и тяхното приложение като хербициди - Google Patents
4-бензил изоксазолови производни, метод за получаването им и тяхното приложение като хербициди Download PDFInfo
- Publication number
- BG60913B1 BG60913B1 BG94965A BG9496591A BG60913B1 BG 60913 B1 BG60913 B1 BG 60913B1 BG 94965 A BG94965 A BG 94965A BG 9496591 A BG9496591 A BG 9496591A BG 60913 B1 BG60913 B1 BG 60913B1
- Authority
- BG
- Bulgaria
- Prior art keywords
- group
- methyl
- cyclopropylisoxazole
- hydroxy
- compound
- Prior art date
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- 238000000034 method Methods 0.000 title claims abstract description 18
- YIOURGVFVDIGQY-UHFFFAOYSA-N 4-benzyl-1,2-oxazole Chemical class C=1C=CC=CC=1CC=1C=NOC=1 YIOURGVFVDIGQY-UHFFFAOYSA-N 0.000 title claims abstract description 7
- 238000002360 preparation method Methods 0.000 title claims abstract description 6
- 239000004009 herbicide Substances 0.000 title description 6
- 150000001875 compounds Chemical class 0.000 claims description 143
- 239000000203 mixture Substances 0.000 claims description 76
- -1 NR J R 4 Chemical group 0.000 claims description 55
- 241000196324 Embryophyta Species 0.000 claims description 51
- 125000005843 halogen group Chemical group 0.000 claims description 43
- 125000004432 carbon atom Chemical group C* 0.000 claims description 38
- 230000002363 herbicidal effect Effects 0.000 claims description 38
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 27
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 239000003085 diluting agent Substances 0.000 claims description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 18
- 239000004094 surface-active agent Substances 0.000 claims description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 17
- 239000007788 liquid Substances 0.000 claims description 17
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 16
- 238000006243 chemical reaction Methods 0.000 claims description 15
- 239000012442 inert solvent Substances 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 229910052740 iodine Inorganic materials 0.000 claims description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 239000013543 active substance Substances 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 239000012141 concentrate Substances 0.000 claims description 10
- 239000000460 chlorine Chemical group 0.000 claims description 9
- 125000004185 ester group Chemical group 0.000 claims description 9
- 229910052736 halogen Inorganic materials 0.000 claims description 9
- 150000002367 halogens Chemical group 0.000 claims description 9
- 239000000843 powder Substances 0.000 claims description 9
- 229910052801 chlorine Chemical group 0.000 claims description 8
- 125000002252 acyl group Chemical group 0.000 claims description 7
- 125000004122 cyclic group Chemical group 0.000 claims description 7
- 150000002545 isoxazoles Chemical class 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 125000003172 aldehyde group Chemical group 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- 239000003377 acid catalyst Substances 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 239000002585 base Substances 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 claims description 5
- 238000009472 formulation Methods 0.000 claims description 5
- 239000008187 granular material Substances 0.000 claims description 5
- LSHRTCCDTJBGKP-UHFFFAOYSA-N (5-cyclopropyl-1,2-oxazol-4-yl)-[2-nitro-4-(trifluoromethyl)phenyl]methanol Chemical compound C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1C(O)C=1C=NOC=1C1CC1 LSHRTCCDTJBGKP-UHFFFAOYSA-N 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 4
- 239000007900 aqueous suspension Substances 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 claims description 4
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 4
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 4
- JTLZJWSIQXXYSR-UHFFFAOYSA-N 1-(5-cyclopropyl-1,2-oxazol-4-yl)-n,n-dimethyl-1-[2-nitro-4-(trifluoromethyl)phenyl]methanamine Chemical compound C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1C(N(C)C)C=1C=NOC=1C1CC1 JTLZJWSIQXXYSR-UHFFFAOYSA-N 0.000 claims description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 3
- ZTPDBCPCGFKVGX-UHFFFAOYSA-N 4-[(2-chloro-4-methylsulfonylphenyl)-methoxymethyl]-5-cyclopropyl-1,2-oxazole Chemical compound C=1C=C(S(C)(=O)=O)C=C(Cl)C=1C(OC)C=1C=NOC=1C1CC1 ZTPDBCPCGFKVGX-UHFFFAOYSA-N 0.000 claims description 3
- ZOCPFOUEPWZRLK-UHFFFAOYSA-N 4-[bromo-[2-nitro-4-(trifluoromethyl)phenyl]methyl]-5-cyclopropyl-1,2-oxazole Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=CC=C1C(Br)C1=C(C2CC2)ON=C1 ZOCPFOUEPWZRLK-UHFFFAOYSA-N 0.000 claims description 3
- SCJSPWKNSJKEOP-UHFFFAOYSA-N 4-[bromo-[4-methylsulfonyl-2-(trifluoromethyl)phenyl]methyl]-5-cyclopropyl-1,2-oxazole Chemical compound FC(F)(F)C1=CC(S(=O)(=O)C)=CC=C1C(Br)C1=C(C2CC2)ON=C1 SCJSPWKNSJKEOP-UHFFFAOYSA-N 0.000 claims description 3
- CWWVHHITOJGDDM-UHFFFAOYSA-N 4-[chloro-[4-methylsulfonyl-2-(trifluoromethyl)phenyl]methyl]-5-cyclopropyl-1,2-oxazole Chemical compound FC(F)(F)C1=CC(S(=O)(=O)C)=CC=C1C(Cl)C1=C(C2CC2)ON=C1 CWWVHHITOJGDDM-UHFFFAOYSA-N 0.000 claims description 3
- RNELMQKHJCVRHQ-UHFFFAOYSA-N 5-cyclopropyl-4-[methoxy-[4-methylsulfonyl-2-(trifluoromethyl)phenyl]methyl]-1,2-oxazole Chemical compound C=1C=C(S(C)(=O)=O)C=C(C(F)(F)F)C=1C(OC)C=1C=NOC=1C1CC1 RNELMQKHJCVRHQ-UHFFFAOYSA-N 0.000 claims description 3
- 150000001299 aldehydes Chemical class 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 239000003153 chemical reaction reagent Substances 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 230000007062 hydrolysis Effects 0.000 claims description 3
- 238000006460 hydrolysis reaction Methods 0.000 claims description 3
- 150000002443 hydroxylamines Chemical class 0.000 claims description 3
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 125000006413 ring segment Chemical group 0.000 claims description 3
- 239000004550 soluble concentrate Substances 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 239000004546 suspension concentrate Substances 0.000 claims description 3
- 239000004563 wettable powder Substances 0.000 claims description 3
- JOCUKUSKSRAOIO-UHFFFAOYSA-N (2-bromo-4-methylsulfonylphenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methanol Chemical compound BrC1=CC(S(=O)(=O)C)=CC=C1C(O)C1=C(C2CC2)ON=C1 JOCUKUSKSRAOIO-UHFFFAOYSA-N 0.000 claims description 2
- ABSACKYDPHGGLG-UHFFFAOYSA-N (2-chloro-3-ethoxy-4-ethylsulfonylphenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methanol Chemical compound C1=C(S(=O)(=O)CC)C(OCC)=C(Cl)C(C(O)C2=C(ON=C2)C2CC2)=C1 ABSACKYDPHGGLG-UHFFFAOYSA-N 0.000 claims description 2
- CIMPLWKXXNDQIK-UHFFFAOYSA-N (2-chloro-3-ethoxy-4-ethylsulfonylphenyl)-(5-methyl-1,2-oxazol-4-yl)methanol Chemical compound C1=C(S(=O)(=O)CC)C(OCC)=C(Cl)C(C(O)C2=C(ON=C2)C)=C1 CIMPLWKXXNDQIK-UHFFFAOYSA-N 0.000 claims description 2
- HSGZRLNVGJYNLI-UHFFFAOYSA-N (2-chloro-4-fluorophenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methanol Chemical compound C=1C=C(F)C=C(Cl)C=1C(O)C=1C=NOC=1C1CC1 HSGZRLNVGJYNLI-UHFFFAOYSA-N 0.000 claims description 2
- SAXDVAYURPJSGD-UHFFFAOYSA-N (2-chloro-4-methylsulfinylphenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methanol Chemical compound ClC1=CC(S(=O)C)=CC=C1C(O)C1=C(C2CC2)ON=C1 SAXDVAYURPJSGD-UHFFFAOYSA-N 0.000 claims description 2
- JTDRONLBVQTVJV-UHFFFAOYSA-N (2-chloro-4-methylsulfonylphenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methanol Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(O)C1=C(C2CC2)ON=C1 JTDRONLBVQTVJV-UHFFFAOYSA-N 0.000 claims description 2
- PKIIPXRVQHZVTP-UHFFFAOYSA-N (4-bromo-2-methylsulfonylphenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methanol Chemical compound CS(=O)(=O)C1=CC(Br)=CC=C1C(O)C1=C(C2CC2)ON=C1 PKIIPXRVQHZVTP-UHFFFAOYSA-N 0.000 claims description 2
- QMOIWVKQXYSZTR-UHFFFAOYSA-N (4-chloro-2-methylsulfonylphenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methanol Chemical compound CS(=O)(=O)C1=CC(Cl)=CC=C1C(O)C1=C(C2CC2)ON=C1 QMOIWVKQXYSZTR-UHFFFAOYSA-N 0.000 claims description 2
- VWEBOGTUVKKTTE-UHFFFAOYSA-N (4-chloro-2-methylsulfonylphenyl)-(5-propan-2-yl-1,2-oxazol-4-yl)methanol Chemical compound O1N=CC(C(O)C=2C(=CC(Cl)=CC=2)S(C)(=O)=O)=C1C(C)C VWEBOGTUVKKTTE-UHFFFAOYSA-N 0.000 claims description 2
- MKLRVCBIOKLTTD-UHFFFAOYSA-N (4-chloro-2-methylsulfonylphenyl)-[5-(1-methylcyclopropyl)-1,2-oxazol-4-yl]methanol Chemical compound O1N=CC(C(O)C=2C(=CC(Cl)=CC=2)S(C)(=O)=O)=C1C1(C)CC1 MKLRVCBIOKLTTD-UHFFFAOYSA-N 0.000 claims description 2
- SRJCOCYMFCJWGE-UHFFFAOYSA-N (5-cyclopropyl-1,2-oxazol-4-yl)-(2-fluoro-4-methylsulfonylphenyl)methanol Chemical compound FC1=CC(S(=O)(=O)C)=CC=C1C(O)C1=C(C2CC2)ON=C1 SRJCOCYMFCJWGE-UHFFFAOYSA-N 0.000 claims description 2
- SDOBSBSPBDAWGO-UHFFFAOYSA-N (5-cyclopropyl-1,2-oxazol-4-yl)-(2-methyl-4-methylsulfonylphenyl)methanol Chemical compound CC1=CC(S(C)(=O)=O)=CC=C1C(O)C1=C(C2CC2)ON=C1 SDOBSBSPBDAWGO-UHFFFAOYSA-N 0.000 claims description 2
- DQZWJTHMYBEQHG-UHFFFAOYSA-N (5-cyclopropyl-1,2-oxazol-4-yl)-(2-methylsulfonylphenyl)methanol Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)C1=C(C2CC2)ON=C1 DQZWJTHMYBEQHG-UHFFFAOYSA-N 0.000 claims description 2
- BOBVFCSUEGHFOP-UHFFFAOYSA-N (5-cyclopropyl-1,2-oxazol-4-yl)-(4-methyl-2-nitrophenyl)methanol Chemical compound [O-][N+](=O)C1=CC(C)=CC=C1C(O)C1=C(C2CC2)ON=C1 BOBVFCSUEGHFOP-UHFFFAOYSA-N 0.000 claims description 2
- AJLHLGPHAZYDON-UHFFFAOYSA-N (5-cyclopropyl-1,2-oxazol-4-yl)-[4-methylsulfonyl-2-(trifluoromethyl)phenyl]methanol Chemical compound FC(F)(F)C1=CC(S(=O)(=O)C)=CC=C1C(O)C1=C(C2CC2)ON=C1 AJLHLGPHAZYDON-UHFFFAOYSA-N 0.000 claims description 2
- JRAKRHMYMKCWJV-UHFFFAOYSA-N (5-methyl-1,2-oxazol-4-yl)-[2-nitro-4-(trifluoromethyl)phenyl]methanol Chemical compound O1N=CC(C(O)C=2C(=CC(=CC=2)C(F)(F)F)[N+]([O-])=O)=C1C JRAKRHMYMKCWJV-UHFFFAOYSA-N 0.000 claims description 2
- 125000001607 1,2,3-triazol-1-yl group Chemical group [*]N1N=NC([H])=C1[H] 0.000 claims description 2
- AFISFTMXPSCNLB-UHFFFAOYSA-N 4-[chloro-[2-nitro-4-(trifluoromethyl)phenyl]methyl]-5-cyclopropyl-1,2-oxazole Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=CC=C1C(Cl)C1=C(C2CC2)ON=C1 AFISFTMXPSCNLB-UHFFFAOYSA-N 0.000 claims description 2
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 2
- JTFNNRZALBWRMW-UHFFFAOYSA-N 5-cyclopropyl-4-[methoxy-[2-nitro-4-(trifluoromethyl)phenyl]methyl]-1,2-oxazole Chemical compound C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1C(OC)C=1C=NOC=1C1CC1 JTFNNRZALBWRMW-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- AXAUPXQTZQMEFA-UHFFFAOYSA-N [(5-cyclopropyl-1,2-oxazol-4-yl)-[2-nitro-4-(trifluoromethyl)phenyl]methyl] acetate Chemical compound C=1C=C(C(F)(F)F)C=C([N+]([O-])=O)C=1C(OC(=O)C)C=1C=NOC=1C1CC1 AXAUPXQTZQMEFA-UHFFFAOYSA-N 0.000 claims description 2
- BSOJSFWJAIFJHT-UHFFFAOYSA-N [(5-cyclopropyl-1,2-oxazol-4-yl)-[4-methylsulfonyl-2-(trifluoromethyl)phenyl]methyl] acetate Chemical compound C=1C=C(S(C)(=O)=O)C=C(C(F)(F)F)C=1C(OC(=O)C)C=1C=NOC=1C1CC1 BSOJSFWJAIFJHT-UHFFFAOYSA-N 0.000 claims description 2
- 150000003855 acyl compounds Chemical class 0.000 claims description 2
- 125000004442 acylamino group Chemical group 0.000 claims description 2
- 125000004423 acyloxy group Chemical group 0.000 claims description 2
- 229910001508 alkali metal halide Inorganic materials 0.000 claims description 2
- 150000008045 alkali metal halides Chemical class 0.000 claims description 2
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 125000003368 amide group Chemical group 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- 150000001721 carbon Chemical group 0.000 claims description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 2
- HRKQOINLCJTGBK-UHFFFAOYSA-N dihydroxidosulfur Chemical compound OSO HRKQOINLCJTGBK-UHFFFAOYSA-N 0.000 claims description 2
- 239000004495 emulsifiable concentrate Substances 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 150000002366 halogen compounds Chemical class 0.000 claims description 2
- 230000002140 halogenating effect Effects 0.000 claims description 2
- 125000002962 imidazol-1-yl group Chemical group [*]N1C([H])=NC([H])=C1[H] 0.000 claims description 2
- 239000012038 nucleophile Substances 0.000 claims description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
- 125000004353 pyrazol-1-yl group Chemical group [H]C1=NN(*)C([H])=C1[H] 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 150000002902 organometallic compounds Chemical class 0.000 claims 2
- ROZDKEVLQIYXCZ-UHFFFAOYSA-N (5-cyclopropyl-1,2-oxazol-4-yl)-[2-methylsulfonyl-4-(trifluoromethyl)phenyl]methanol Chemical compound CS(=O)(=O)C1=CC(C(F)(F)F)=CC=C1C(O)C1=C(C2CC2)ON=C1 ROZDKEVLQIYXCZ-UHFFFAOYSA-N 0.000 claims 1
- 125000001401 1,2,4-triazol-4-yl group Chemical group N=1N=C([H])N([*])C=1[H] 0.000 claims 1
- 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- WHLNOTKZOZATEP-UHFFFAOYSA-N [(2-chloro-4-methylsulfonylphenyl)-(5-cyclopropyl-1,2-oxazol-4-yl)methyl] acetate Chemical compound C=1C=C(S(C)(=O)=O)C=C(Cl)C=1C(OC(=O)C)C=1C=NOC=1C1CC1 WHLNOTKZOZATEP-UHFFFAOYSA-N 0.000 claims 1
- ITCHYDLVUCAIHX-UHFFFAOYSA-N [(5-cyclopropyl-1,2-oxazol-4-yl)-[4-methylsulfonyl-2-(trifluoromethyl)phenyl]methyl] 2,2,2-trifluoroacetate Chemical compound FC(F)(F)C1=CC(S(=O)(=O)C)=CC=C1C(OC(=O)C(F)(F)F)C1=C(C2CC2)ON=C1 ITCHYDLVUCAIHX-UHFFFAOYSA-N 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 238000012272 crop production Methods 0.000 claims 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 79
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 42
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 36
- 239000000243 solution Substances 0.000 description 31
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 31
- 238000005481 NMR spectroscopy Methods 0.000 description 26
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 24
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 24
- 239000007787 solid Substances 0.000 description 22
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 20
- 125000001309 chloro group Chemical group Cl* 0.000 description 20
- 239000000706 filtrate Substances 0.000 description 16
- 239000002904 solvent Substances 0.000 description 15
- 230000000052 comparative effect Effects 0.000 description 12
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 description 11
- 239000002689 soil Substances 0.000 description 11
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 239000000969 carrier Substances 0.000 description 10
- 239000003208 petroleum Substances 0.000 description 10
- 238000010992 reflux Methods 0.000 description 10
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- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 9
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- 235000008504 concentrate Nutrition 0.000 description 7
- 230000035784 germination Effects 0.000 description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
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- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000011111 cardboard Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- JXCGFZXSOMJFOA-UHFFFAOYSA-N chlorotoluron Chemical compound CN(C)C(=O)NC1=CC=C(C)C(Cl)=C1 JXCGFZXSOMJFOA-UHFFFAOYSA-N 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- ZOOSILUVXHVRJE-UHFFFAOYSA-N cyclopropanecarbonyl chloride Chemical compound ClC(=O)C1CC1 ZOOSILUVXHVRJE-UHFFFAOYSA-N 0.000 description 1
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 description 1
- 229960005424 cypermethrin Drugs 0.000 description 1
- 229960003887 dichlorophen Drugs 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- UZUODNWWWUQRIR-UHFFFAOYSA-L disodium;3-aminonaphthalene-1,5-disulfonate Chemical compound [Na+].[Na+].C1=CC=C(S([O-])(=O)=O)C2=CC(N)=CC(S([O-])(=O)=O)=C21 UZUODNWWWUQRIR-UHFFFAOYSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- JYNAPIWQOHMXNB-UHFFFAOYSA-N imidazol-1-yl-(1-methylcyclopropyl)methanone Chemical compound C1=CN=CN1C(=O)C1(C)CC1 JYNAPIWQOHMXNB-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- PUIYMUZLKQOUOZ-UHFFFAOYSA-N isoproturon Chemical compound CC(C)C1=CC=C(NC(=O)N(C)C)C=C1 PUIYMUZLKQOUOZ-UHFFFAOYSA-N 0.000 description 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 1
- 125000000842 isoxazolyl group Chemical group 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- CFHGBZLNZZVTAY-UHFFFAOYSA-N lawesson's reagent Chemical compound C1=CC(OC)=CC=C1P1(=S)SP(=S)(C=2C=CC(OC)=CC=2)S1 CFHGBZLNZZVTAY-UHFFFAOYSA-N 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- GXHFUVWIGNLZSC-UHFFFAOYSA-N meldrum's acid Chemical compound CC1(C)OC(=O)CC(=O)O1 GXHFUVWIGNLZSC-UHFFFAOYSA-N 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000002663 nebulization Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical class CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 235000020636 oyster Nutrition 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
- 229960000490 permethrin Drugs 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- KOOZJKASKDTFJS-UHFFFAOYSA-N tert-butyl 2-[2-nitro-4-(trifluoromethyl)benzoyl]-3-oxobutanoate Chemical compound CC(C)(C)OC(=O)C(C(=O)C)C(=O)C1=CC=C(C(F)(F)F)C=C1[N+]([O-])=O KOOZJKASKDTFJS-UHFFFAOYSA-N 0.000 description 1
- HOHBQWITMXOSOW-UHFFFAOYSA-N tert-butyl 2-trimethylsilylacetate Chemical compound CC(C)(C)OC(=O)C[Si](C)(C)C HOHBQWITMXOSOW-UHFFFAOYSA-N 0.000 description 1
- CHBUAVKFDIVTMW-UHFFFAOYSA-N tert-butyl 3-(1-methylcyclopropyl)-3-oxopropanoate Chemical compound CC(C)(C)OC(=O)CC(=O)C1(C)CC1 CHBUAVKFDIVTMW-UHFFFAOYSA-N 0.000 description 1
- QTEMECAXQLRGCH-UHFFFAOYSA-N tert-butyl 3-cyclopropyl-2-[[2-nitro-4-(trifluoromethyl)phenyl]methyl]-3-oxopropanoate Chemical compound C1(CC1)C(C(C(=O)OC(C)(C)C)CC1=C(C=C(C=C1)C(F)(F)F)[N+](=O)[O-])=O QTEMECAXQLRGCH-UHFFFAOYSA-N 0.000 description 1
- JKUYRAMKJLMYLO-UHFFFAOYSA-N tert-butyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OC(C)(C)C JKUYRAMKJLMYLO-UHFFFAOYSA-N 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- 125000005490 tosylate group Chemical group 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 239000000052 vinegar Chemical group 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/14—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Prostheses (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB909017539A GB9017539D0 (en) | 1990-08-10 | 1990-08-10 | New compositions of matter |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BG94965A BG94965A (bg) | 1993-12-24 |
| BG60913B1 true BG60913B1 (bg) | 1996-06-28 |
Family
ID=10680447
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BG94965A BG60913B1 (bg) | 1990-08-10 | 1991-08-08 | 4-бензил изоксазолови производни, метод за получаването им и тяхното приложение като хербициди |
Country Status (31)
| Country | Link |
|---|---|
| EP (1) | EP0470856B1 (de) |
| JP (1) | JPH05345770A (de) |
| KR (1) | KR920004365A (de) |
| CN (1) | CN1058777A (de) |
| AT (1) | ATE128972T1 (de) |
| AU (1) | AU643310B2 (de) |
| BG (1) | BG60913B1 (de) |
| BR (1) | BR9103433A (de) |
| CA (1) | CA2048705A1 (de) |
| CZ (1) | CZ282110B6 (de) |
| DE (1) | DE69113721T2 (de) |
| DK (1) | DK0470856T3 (de) |
| EG (1) | EG19513A (de) |
| ES (1) | ES2077806T3 (de) |
| FI (1) | FI913782A (de) |
| GB (1) | GB9017539D0 (de) |
| GR (1) | GR3018526T3 (de) |
| HU (1) | HUT58188A (de) |
| IE (1) | IE74866B1 (de) |
| IL (1) | IL99132A (de) |
| MA (1) | MA22252A1 (de) |
| MY (1) | MY107611A (de) |
| NZ (1) | NZ239305A (de) |
| OA (1) | OA09391A (de) |
| PH (1) | PH30440A (de) |
| PT (1) | PT98627B (de) |
| RO (1) | RO109941B1 (de) |
| RU (1) | RU2055072C1 (de) |
| TR (1) | TR27003A (de) |
| YU (1) | YU48471B (de) |
| ZA (1) | ZA916305B (de) |
Families Citing this family (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9025469D0 (en) * | 1990-11-22 | 1991-01-09 | Rhone Poulenc Agriculture | New compositions of matter |
| JPH0570407A (ja) * | 1991-09-17 | 1993-03-23 | Fuji Photo Film Co Ltd | シクロプロパンカルボニル酢酸エステル |
| US5334753A (en) * | 1992-03-12 | 1994-08-02 | Rhone-Poulenc Agriculture Ltd | Processes for preparing ortho-substituted benzoic acids |
| JPH08504781A (ja) * | 1992-12-18 | 1996-05-21 | ローヌ−プーラン・アグリカルチヤー・リミテツド | ４−ベンゾイルイソオキサゾール誘導体及び除草剤としてのその使用 |
| GB9302049D0 (en) * | 1993-02-03 | 1993-03-24 | Rhone Poulenc Agriculture | Compositions of new matter |
| GB9302071D0 (en) * | 1993-02-03 | 1993-03-24 | Rhone Poulenc Agriculture | Compositions of matter |
| CA2117413C (en) * | 1993-07-30 | 2006-11-21 | Neil Geach | Herbicidal isoxazole-4-yl-methanone derivatives |
| DE19548428C1 (de) * | 1995-12-22 | 1997-08-28 | Hoechst Ag | 2-Alkylmerkapto-4-(trifluormethyl)-benzoesäureester sowie ein Verfahren zu ihrer Herstellung |
| US6297198B1 (en) | 1996-05-14 | 2001-10-02 | Syngenta Participations Ag | Isoxazole derivatives and their use as herbicides |
| DE69812356T2 (de) * | 1997-06-03 | 2003-08-28 | Eastman Chemical Co., Kingsport | Verfahren zur herstellung von thioether substituierten aromatischen ketonen |
| DE69808288T2 (de) * | 1997-06-03 | 2003-01-16 | Eastman Chemical Co., Kingsport | Verfahren zur herstellung von 1,3-dicarbonylverbindungen |
| EP1009727A1 (de) | 1997-06-03 | 2000-06-21 | Eastman Chemical Company | Katalysator für die oxidative nef-reaktion unter verwendung von basischen wasserperoxiden |
| US6096929A (en) * | 1998-06-02 | 2000-08-01 | Eastman Kodak Company | Process for the preparation of thioether-substituted aromatic ketones |
| ES2405266T3 (es) | 1998-08-13 | 2013-05-30 | Bayer Cropscience Ag | Agentes herbicidas para cultivos de maíz tolerantes o resistentes |
| US6337418B1 (en) | 1999-04-09 | 2002-01-08 | Eastman Chemical Co. | Preparation of C1-C5 alkyl esters of nitro or thioether substituted aromatic carboxylic acids |
| FR2815969B1 (fr) | 2000-10-30 | 2004-12-10 | Aventis Cropscience Sa | Plantes tolerantes aux herbicides par contournement de voie metabolique |
| CA2457575C (en) | 2001-08-17 | 2010-12-21 | Sankyo Agro Company, Limited | 3-phenoxy-4-pyridazinol derivatives and herbicidal composition containing the same |
| FR2844142B1 (fr) | 2002-09-11 | 2007-08-17 | Bayer Cropscience Sa | Plantes transformees a biosynthese de prenylquinones amelioree |
| ITMI20031855A1 (it) * | 2003-09-29 | 2005-03-30 | Isagro Ricerca Srl | Derivati di 1,3-dioni aventi attivita' erbicida. |
| AR074941A1 (es) | 2009-01-07 | 2011-02-23 | Bayer Cropscience Sa | Plantas transplastomicas exentas de marcador de seleccion |
| US8153132B2 (en) | 2009-10-30 | 2012-04-10 | Ms Technologies, Inc. | Antibodies immunoreactive with mutant hydroxypenylpyruvate dioxygenase |
| CN102741415A (zh) | 2010-02-02 | 2012-10-17 | 拜尔农科股份公司 | 使用hppd抑制剂作为选择剂的大豆转化 |
| DE112011101566T5 (de) | 2010-05-04 | 2013-05-08 | Basf Se | Pflanzen mit erhöhter herbizidtoleranz |
| CA2820706C (en) | 2010-12-03 | 2018-05-22 | Ms Technologies, Llc | Optimized expression of glyphosate resistance encoding nucleic acid molecules in plant cells |
| US8648230B2 (en) | 2011-03-18 | 2014-02-11 | Ms Technologies, Llc | Regulatory regions preferentially expressing in non-pollen plant tissue |
| MX344968B (es) | 2012-02-01 | 2017-01-12 | Dow Agrosciences Llc | Peptido de transito al cloroplasto. |
| NZ746567A (en) | 2013-11-04 | 2019-09-27 | Dow Agrosciences Llc | Optimal soybean loci |
| CA2928855A1 (en) | 2013-11-04 | 2015-05-07 | Dow Agrosciences Llc | Optimal maize loci |
| KR102269769B1 (ko) | 2013-11-04 | 2021-06-28 | 코르테바 애그리사이언스 엘엘씨 | 최적 메이즈 유전자좌 |
| TW201527316A (zh) | 2013-12-31 | 2015-07-16 | Dow Agrosciences Llc | 新穎玉米泛素啓動子（五） |
| TW201527313A (zh) | 2013-12-31 | 2015-07-16 | Dow Agrosciences Llc | 新穎玉米泛素啓動子（二） |
| TW201527314A (zh) | 2013-12-31 | 2015-07-16 | Dow Agrosciences Llc | 新穎玉米泛素啓動子（三） |
| TW201527312A (zh) | 2013-12-31 | 2015-07-16 | Dow Agrosciences Llc | 新穎玉米泛素啓動子（一） |
| TW201538518A (zh) | 2014-02-28 | 2015-10-16 | Dow Agrosciences Llc | 藉由嵌合基因調控元件所賦予之根部特異性表現 |
| CN104529924B (zh) * | 2014-12-26 | 2016-03-02 | 江苏中旗作物保护股份有限公司 | 5-环丙基-4-[2-甲硫基-4-(三氟甲基)苯甲酰基]异恶唑的制备方法 |
| CN104817510B (zh) * | 2015-03-10 | 2017-07-07 | 北京颖泰嘉和生物科技股份有限公司 | 一种异噁唑化合物的制备方法 |
| CN107517980A (zh) * | 2016-06-21 | 2017-12-29 | 江苏龙灯化学有限公司 | 一种除草组合物 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR6915465D0 (pt) * | 1969-03-07 | 1973-01-04 | Bayer Ag | Processo para preparar n-benzimidazois substituidos na posicao alfa por heterociclos penta-membrados com atividade antimicotica |
| BE756663A (fr) * | 1969-09-27 | 1971-03-25 | Bayer Ag | Composition destinee a la regulation de la croissance des vegetaux |
| DE1964995A1 (de) * | 1969-12-24 | 1971-07-01 | Bayer Ag | N-Benzyltriazole,Verfahren zu ihrer Herstellung und ihre Verwendung zur Regulierung des Pflanzenwachstums |
| DE2009020C3 (de) * | 1970-02-26 | 1979-09-13 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von N-(l,l,l-trisubstituierten)-Methylazolen |
| DE2016839C3 (de) * | 1970-04-09 | 1979-03-22 | Bayer Ag, 5090 Leverkusen | PhenyM4-phenoxyphenyi)-imidazol-1-yl-methane, Verfahren zu ihrer Herstellung sowie diese Verbindungen enthaltende Arzneimittel |
| DE2754832A1 (de) * | 1977-12-09 | 1979-06-13 | Basf Ag | Verfahren zur herstellung aliphatischer nitriloxide |
| JPS6052713B2 (ja) * | 1978-04-11 | 1985-11-20 | 三共株式会社 | ７−メトキシセフアロスポリン化合物、その製法及びその化合物を主成分とする抗菌剤 |
| US4562187A (en) * | 1985-01-22 | 1985-12-31 | Hoechst-Roussel Pharmaceuticals Inc. | (Isoxazol-3-yl)arylmethanones, compositions and pharmaceutical use |
| JPS6345277A (ja) * | 1986-04-03 | 1988-02-26 | Shionogi & Co Ltd | イソオキサゾリルエタノ−ル誘導体、抗真菌剤および農業用殺菌剤 |
| US4914112A (en) * | 1986-06-03 | 1990-04-03 | Sumitomo Pharmaceuticals Company, Limited | Aminoazole derivatives and their production and use |
| GB9025469D0 (en) * | 1990-11-22 | 1991-01-09 | Rhone Poulenc Agriculture | New compositions of matter |
-
1990
- 1990-08-10 GB GB909017539A patent/GB9017539D0/en active Pending
-
1991
- 1991-08-07 AU AU81678/91A patent/AU643310B2/en not_active Ceased
- 1991-08-07 YU YU135991A patent/YU48471B/sh unknown
- 1991-08-08 CA CA002048705A patent/CA2048705A1/en not_active Abandoned
- 1991-08-08 MA MA22532A patent/MA22252A1/fr unknown
- 1991-08-08 RO RO148219A patent/RO109941B1/ro unknown
- 1991-08-08 IL IL9913291A patent/IL99132A/en active IP Right Grant
- 1991-08-08 NZ NZ239305A patent/NZ239305A/xx unknown
- 1991-08-08 BG BG94965A patent/BG60913B1/bg unknown
- 1991-08-09 TR TR00740/91A patent/TR27003A/xx unknown
- 1991-08-09 HU HU912664A patent/HUT58188A/hu unknown
- 1991-08-09 FI FI913782A patent/FI913782A/fi not_active Application Discontinuation
- 1991-08-09 DK DK91307351.6T patent/DK0470856T3/da active
- 1991-08-09 BR BR919103433A patent/BR9103433A/pt not_active Application Discontinuation
- 1991-08-09 DE DE69113721T patent/DE69113721T2/de not_active Expired - Fee Related
- 1991-08-09 PH PH42916A patent/PH30440A/en unknown
- 1991-08-09 IE IE282991A patent/IE74866B1/en not_active IP Right Cessation
- 1991-08-09 AT AT91307351T patent/ATE128972T1/de not_active IP Right Cessation
- 1991-08-09 CZ CS912473A patent/CZ282110B6/cs unknown
- 1991-08-09 PT PT98627A patent/PT98627B/pt not_active IP Right Cessation
- 1991-08-09 EP EP91307351A patent/EP0470856B1/de not_active Expired - Lifetime
- 1991-08-09 JP JP3200537A patent/JPH05345770A/ja active Pending
- 1991-08-09 ES ES91307351T patent/ES2077806T3/es not_active Expired - Lifetime
- 1991-08-09 OA OA60062A patent/OA09391A/xx unknown
- 1991-08-09 MY MYPI91001442A patent/MY107611A/en unknown
- 1991-08-09 RU SU915001315A patent/RU2055072C1/ru active
- 1991-08-09 ZA ZA916305A patent/ZA916305B/xx unknown
- 1991-08-10 KR KR1019910013828A patent/KR920004365A/ko not_active Application Discontinuation
- 1991-08-10 CN CN91105623A patent/CN1058777A/zh active Pending
- 1991-08-10 EG EG48391A patent/EG19513A/xx active
-
1995
- 1995-12-22 GR GR950403666T patent/GR3018526T3/el unknown
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