NO832269L - Furfurylamider av fenoksy-fenoksy-alkansyrer. - Google Patents
Furfurylamider av fenoksy-fenoksy-alkansyrer.Info
- Publication number
- NO832269L NO832269L NO832269A NO832269A NO832269L NO 832269 L NO832269 L NO 832269L NO 832269 A NO832269 A NO 832269A NO 832269 A NO832269 A NO 832269A NO 832269 L NO832269 L NO 832269L
- Authority
- NO
- Norway
- Prior art keywords
- phenoxy
- nitro
- furfuryl
- chloro
- trifluoromethylphenoxy
- Prior art date
Links
- -1 PHENOXY-PHENOXY Chemical class 0.000 title claims description 19
- 239000002253 acid Substances 0.000 title description 6
- 150000007513 acids Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 48
- 241000196324 Embryophyta Species 0.000 claims description 36
- 239000004009 herbicide Substances 0.000 claims description 30
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical group 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- 230000002363 herbicidal effect Effects 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 4
- 231100000331 toxic Toxicity 0.000 claims description 4
- 230000002588 toxic effect Effects 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- COTCLPDJIXGMIG-UHFFFAOYSA-N 2-[2-bromo-5-(4-bromo-2-cyanophenoxy)phenoxy]-n-butyl-n-(furan-2-ylmethyl)propanamide Chemical compound C=1C(OC=2C(=CC(Br)=CC=2)C#N)=CC=C(Br)C=1OC(C)C(=O)N(CCCC)CC1=CC=CO1 COTCLPDJIXGMIG-UHFFFAOYSA-N 0.000 claims description 3
- LXTHQZHHCQQTHL-UHFFFAOYSA-N 2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenoxy]-n-(furan-2-ylmethyl)propanamide Chemical compound C=1C=COC=1CNC(=O)C(C)OC(C(=CC=1)[N+]([O-])=O)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl LXTHQZHHCQQTHL-UHFFFAOYSA-N 0.000 claims description 3
- PDVRBWVBKVCWJE-UHFFFAOYSA-N 2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenoxy]-n-(oxolan-2-ylmethyl)propanamide Chemical compound C1CCOC1CNC(=O)C(C)OC(C(=CC=1)[N+]([O-])=O)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl PDVRBWVBKVCWJE-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- LMMDRXRHXIWZOR-UHFFFAOYSA-N n-ethyl-2-[5-(4-fluorophenoxy)-2-nitrophenoxy]-n-(furan-2-ylmethyl)propanamide Chemical compound C=1C(OC=2C=CC(F)=CC=2)=CC=C([N+]([O-])=O)C=1OC(C)C(=O)N(CC)CC1=CC=CO1 LMMDRXRHXIWZOR-UHFFFAOYSA-N 0.000 claims description 3
- RDHHBJVOISSQLP-UHFFFAOYSA-N 2-[2-chloro-5-(4-chloro-2-nitrophenoxy)phenoxy]-n-(furan-2-ylmethyl)-n-propylpropanamide Chemical compound C=1C(OC=2C(=CC(Cl)=CC=2)[N+]([O-])=O)=CC=C(Cl)C=1OC(C)C(=O)N(CCC)CC1=CC=CO1 RDHHBJVOISSQLP-UHFFFAOYSA-N 0.000 claims description 2
- YNUWLKNCJMSEJU-UHFFFAOYSA-N 2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenoxy]-n-(furan-2-ylmethyl)-n-methylpropanamide Chemical compound C=1C=COC=1CN(C)C(=O)C(C)OC(C(=CC=1)[N+]([O-])=O)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl YNUWLKNCJMSEJU-UHFFFAOYSA-N 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- CMDQSUGZGQCVJO-UHFFFAOYSA-N 2-[5-[2-bromo-4-(trifluoromethyl)phenoxy]-2-nitrophenoxy]-n-(furan-2-ylmethyl)propanamide Chemical compound C=1C=COC=1CNC(=O)C(C)OC(C(=CC=1)[N+]([O-])=O)=CC=1OC1=CC=C(C(F)(F)F)C=C1Br CMDQSUGZGQCVJO-UHFFFAOYSA-N 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 63
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 60
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 30
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 30
- 239000002904 solvent Substances 0.000 description 26
- 239000000203 mixture Substances 0.000 description 25
- 239000000243 solution Substances 0.000 description 24
- 238000003756 stirring Methods 0.000 description 21
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 20
- 239000011541 reaction mixture Substances 0.000 description 20
- 238000006243 chemical reaction Methods 0.000 description 18
- 238000002360 preparation method Methods 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 14
- 239000011521 glass Substances 0.000 description 11
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 10
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 10
- 235000017557 sodium bicarbonate Nutrition 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000004587 chromatography analysis Methods 0.000 description 9
- 239000003480 eluent Substances 0.000 description 9
- 238000004566 IR spectroscopy Methods 0.000 description 8
- 238000010828 elution Methods 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- 230000006378 damage Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 235000019260 propionic acid Nutrition 0.000 description 6
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 6
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
- 239000000428 dust Substances 0.000 description 5
- DDRPCXLAQZKBJP-UHFFFAOYSA-N furfurylamine Chemical compound NCC1=CC=CO1 DDRPCXLAQZKBJP-UHFFFAOYSA-N 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- 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 description 4
- DARZATKTRWGDQO-UHFFFAOYSA-N 2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenoxy]propanoyl chloride Chemical compound C1=C([N+]([O-])=O)C(OC(C)C(Cl)=O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 DARZATKTRWGDQO-UHFFFAOYSA-N 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- 230000012010 growth Effects 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 241001290610 Abildgaardia Species 0.000 description 3
- 239000002837 defoliant Substances 0.000 description 3
- 239000002274 desiccant Substances 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 3
- 229940080818 propionamide Drugs 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- YUFFSWGQGVEMMI-JLNKQSITSA-N (7Z,10Z,13Z,16Z,19Z)-docosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCCCC(O)=O YUFFSWGQGVEMMI-JLNKQSITSA-N 0.000 description 2
- DGLIOWSKNOCHEX-UHFFFAOYSA-N 1-(furan-2-yl)-n-methylmethanamine Chemical compound CNCC1=CC=CO1 DGLIOWSKNOCHEX-UHFFFAOYSA-N 0.000 description 2
- LBBLOAGORIGTIK-UHFFFAOYSA-N 2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-cyanophenoxy]-n-(furan-2-ylmethyl)hexanamide Chemical compound C=1C=COC=1CNC(=O)C(CCCC)OC(C(=CC=1)C#N)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl LBBLOAGORIGTIK-UHFFFAOYSA-N 0.000 description 2
- IXBPNDWZDKPGKA-UHFFFAOYSA-N 2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenoxy]-n-(furan-2-ylmethyl)butanamide Chemical compound C=1C=COC=1CNC(=O)C(CC)OC(C(=CC=1)[N+]([O-])=O)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl IXBPNDWZDKPGKA-UHFFFAOYSA-N 0.000 description 2
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 241000132536 Cirsium Species 0.000 description 2
- 240000003173 Drymaria cordata Species 0.000 description 2
- 244000248416 Fagopyrum cymosum Species 0.000 description 2
- 240000000982 Malva neglecta Species 0.000 description 2
- 235000000060 Malva neglecta Nutrition 0.000 description 2
- 244000042664 Matricaria chamomilla Species 0.000 description 2
- OKUGPJPKMAEJOE-UHFFFAOYSA-N S-propyl dipropylcarbamothioate Chemical compound CCCSC(=O)N(CCC)CCC OKUGPJPKMAEJOE-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 244000062793 Sorghum vulgare Species 0.000 description 2
- PNRAZZZISDRWMV-UHFFFAOYSA-N Terbucarb Chemical compound CNC(=O)OC1=C(C(C)(C)C)C=C(C)C=C1C(C)(C)C PNRAZZZISDRWMV-UHFFFAOYSA-N 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- OGGXGZAMXPVRFZ-UHFFFAOYSA-N dimethylarsinic acid Chemical compound C[As](C)(O)=O OGGXGZAMXPVRFZ-UHFFFAOYSA-N 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 244000144972 livestock Species 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- CBVNYJPAGHUWKC-UHFFFAOYSA-N n-(furan-2-ylmethyl)ethanamine Chemical compound CCNCC1=CC=CO1 CBVNYJPAGHUWKC-UHFFFAOYSA-N 0.000 description 2
- LPPWAQZJYMWSHG-UHFFFAOYSA-N n-(furan-2-ylmethyl)propan-1-amine Chemical compound CCCNCC1=CC=CO1 LPPWAQZJYMWSHG-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 238000005191 phase separation Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 244000045561 useful plants Species 0.000 description 2
- GXEKYRXVRROBEV-FBXFSONDSA-N (1r,2s,3r,4s)-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid Chemical compound C1C[C@@H]2[C@@H](C(O)=O)[C@@H](C(=O)O)[C@H]1O2 GXEKYRXVRROBEV-FBXFSONDSA-N 0.000 description 1
- BIYFBWRLDKOYMU-UHFFFAOYSA-N 1-(3,4-dichlorophenyl)-2-(ethylamino)propan-1-one Chemical compound CCNC(C)C(=O)C1=CC=C(Cl)C(Cl)=C1 BIYFBWRLDKOYMU-UHFFFAOYSA-N 0.000 description 1
- WLKSPGHQGFFKGE-UHFFFAOYSA-N 1-chloropropan-2-yl n-(3-chlorophenyl)carbamate Chemical compound ClCC(C)OC(=O)NC1=CC=CC(Cl)=C1 WLKSPGHQGFFKGE-UHFFFAOYSA-N 0.000 description 1
- NEBPTMCRLHKPOB-UHFFFAOYSA-N 2,2-diphenylacetonitrile Chemical compound C=1C=CC=CC=1C(C#N)C1=CC=CC=C1 NEBPTMCRLHKPOB-UHFFFAOYSA-N 0.000 description 1
- XTVIFVALDYTCLL-UHFFFAOYSA-N 2,3,5-trichloro-1h-pyridin-4-one Chemical compound ClC1=CNC(Cl)=C(Cl)C1=O XTVIFVALDYTCLL-UHFFFAOYSA-N 0.000 description 1
- SVPKNMBRVBMTLB-UHFFFAOYSA-N 2,3-dichloronaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(Cl)=C(Cl)C(=O)C2=C1 SVPKNMBRVBMTLB-UHFFFAOYSA-N 0.000 description 1
- GKFWNPPZHDYVLI-UHFFFAOYSA-N 2,3-dichloropropanoic acid Chemical compound OC(=O)C(Cl)CCl GKFWNPPZHDYVLI-UHFFFAOYSA-N 0.000 description 1
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 description 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
- KBQPYERMRVPJDC-UHFFFAOYSA-N 2,4-dichloro-3-nitrobenzoic acid Chemical compound OC(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1Cl KBQPYERMRVPJDC-UHFFFAOYSA-N 0.000 description 1
- PSOZMUMWCXLRKX-UHFFFAOYSA-N 2,4-dinitro-6-pentan-2-ylphenol Chemical compound CCCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O PSOZMUMWCXLRKX-UHFFFAOYSA-N 0.000 description 1
- YOYAIZYFCNQIRF-UHFFFAOYSA-N 2,6-dichlorobenzonitrile Chemical compound ClC1=CC=CC(Cl)=C1C#N YOYAIZYFCNQIRF-UHFFFAOYSA-N 0.000 description 1
- LGURYBCSJPXHTF-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)ethyl benzoate Chemical compound ClC1=CC(Cl)=CC=C1OCCOC(=O)C1=CC=CC=C1 LGURYBCSJPXHTF-UHFFFAOYSA-N 0.000 description 1
- LZIYRGOPGKPMQP-UHFFFAOYSA-N 2-(2,6-dichlorophenyl)-2-methoxyacetic acid Chemical compound COC(C(O)=O)C1=C(Cl)C=CC=C1Cl LZIYRGOPGKPMQP-UHFFFAOYSA-N 0.000 description 1
- IZMAHTNKZIVDCC-UHFFFAOYSA-N 2-(3,4,6-trichloro-2-methoxyphenyl)acetic acid Chemical compound COC1=C(Cl)C(Cl)=CC(Cl)=C1CC(O)=O IZMAHTNKZIVDCC-UHFFFAOYSA-N 0.000 description 1
- AKQARCRBBSITGB-UHFFFAOYSA-N 2-(3,4-dichlorophenyl)-4-methyl-1,2,4-oxadiazolidine Chemical compound C1N(C)CON1C1=CC=C(Cl)C(Cl)=C1 AKQARCRBBSITGB-UHFFFAOYSA-N 0.000 description 1
- OWZPCEFYPSAJFR-UHFFFAOYSA-N 2-(butan-2-yl)-4,6-dinitrophenol Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O OWZPCEFYPSAJFR-UHFFFAOYSA-N 0.000 description 1
- FLFZMKJHDIMPLK-UHFFFAOYSA-N 2-[2-bromo-5-(4-bromo-2-cyanophenoxy)phenoxy]propanoyl chloride Chemical compound C1=C(Br)C(OC(C)C(Cl)=O)=CC(OC=2C(=CC(Br)=CC=2)C#N)=C1 FLFZMKJHDIMPLK-UHFFFAOYSA-N 0.000 description 1
- MATIRZFVMTVEAR-UHFFFAOYSA-N 2-[2-chloro-5-(4-chloro-2-nitrophenoxy)phenoxy]propanoyl chloride Chemical compound C1=C(Cl)C(OC(C)C(Cl)=O)=CC(OC=2C(=CC(Cl)=CC=2)[N+]([O-])=O)=C1 MATIRZFVMTVEAR-UHFFFAOYSA-N 0.000 description 1
- NIQYKHXXLVNJBD-UHFFFAOYSA-N 2-[2-cyano-5-(4-fluorophenoxy)phenoxy]propanoic acid Chemical compound C1=C(C#N)C(OC(C)C(O)=O)=CC(OC=2C=CC(F)=CC=2)=C1 NIQYKHXXLVNJBD-UHFFFAOYSA-N 0.000 description 1
- CJLHVLGILRDYRC-UHFFFAOYSA-N 2-[5-(4-fluorophenoxy)-2-nitrophenoxy]propanoyl chloride Chemical compound C1=C([N+]([O-])=O)C(OC(C)C(Cl)=O)=CC(OC=2C=CC(F)=CC=2)=C1 CJLHVLGILRDYRC-UHFFFAOYSA-N 0.000 description 1
- SNWGQDVSENCLBM-UHFFFAOYSA-N 2-[5-(4-iodophenoxy)-2-nitrophenoxy]propanoic acid Chemical compound C1=C([N+]([O-])=O)C(OC(C)C(O)=O)=CC(OC=2C=CC(I)=CC=2)=C1 SNWGQDVSENCLBM-UHFFFAOYSA-N 0.000 description 1
- XPDRACKMLPTGQL-UHFFFAOYSA-N 2-[5-[2-bromo-4-(trifluoromethyl)phenoxy]-2-nitrophenoxy]propanoyl chloride Chemical compound C1=C([N+]([O-])=O)C(OC(C)C(Cl)=O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Br)=C1 XPDRACKMLPTGQL-UHFFFAOYSA-N 0.000 description 1
- VVMYESDTMCIGIS-UHFFFAOYSA-N 2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-cyanophenoxy]hexanoyl chloride Chemical compound C1=C(C#N)C(OC(CCCC)C(Cl)=O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 VVMYESDTMCIGIS-UHFFFAOYSA-N 0.000 description 1
- KWGXEWMYPOQAGT-UHFFFAOYSA-N 2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenoxy]-n-(furan-2-ylmethyl)-n-methylpentanamide Chemical compound C=1C=COC=1CN(C)C(=O)C(CCC)OC(C(=CC=1)[N+]([O-])=O)=CC=1OC1=CC=C(C(F)(F)F)C=C1Cl KWGXEWMYPOQAGT-UHFFFAOYSA-N 0.000 description 1
- AYMJPOLWBACNCX-UHFFFAOYSA-N 2-[5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrophenoxy]propanoic acid Chemical compound C1=C([N+]([O-])=O)C(OC(C)C(O)=O)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 AYMJPOLWBACNCX-UHFFFAOYSA-N 0.000 description 1
- YMQRPXBBBOXHNZ-UHFFFAOYSA-N 2-chloro-1-morpholin-4-ylethanone Chemical compound ClCC(=O)N1CCOCC1 YMQRPXBBBOXHNZ-UHFFFAOYSA-N 0.000 description 1
- NSWLMOHUXYULKL-UHFFFAOYSA-N 2-chloro-1-piperidin-1-ylethanone Chemical compound ClCC(=O)N1CCCCC1 NSWLMOHUXYULKL-UHFFFAOYSA-N 0.000 description 1
- CQQUWTMMFMJEFE-UHFFFAOYSA-N 2-chloro-n,n-diethylacetamide Chemical compound CCN(CC)C(=O)CCl CQQUWTMMFMJEFE-UHFFFAOYSA-N 0.000 description 1
- XBPPLECAZBTMMK-UHFFFAOYSA-N 2-chloro-n,n-dimethylacetamide Chemical compound CN(C)C(=O)CCl XBPPLECAZBTMMK-UHFFFAOYSA-N 0.000 description 1
- GYPNJSBBOATUPK-UHFFFAOYSA-N 2-chloro-n-propan-2-ylacetamide Chemical compound CC(C)NC(=O)CCl GYPNJSBBOATUPK-UHFFFAOYSA-N 0.000 description 1
- GYJQWEIGUGMFMU-UHFFFAOYSA-N 2-chloroethyl n-(3-chlorophenyl)carbamate Chemical compound ClCCOC(=O)NC1=CC=CC(Cl)=C1 GYJQWEIGUGMFMU-UHFFFAOYSA-N 0.000 description 1
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
- WRFWAYDBNCOWRA-UHFFFAOYSA-N 3,4-dichloro-1-(6-iodo-4-oxo-2-thiophen-2-ylquinazolin-3-yl)pyrrole-2,5-dione Chemical compound O=C1C(Cl)=C(Cl)C(=O)N1N1C(=O)C2=CC(I)=CC=C2N=C1C1=CC=CS1 WRFWAYDBNCOWRA-UHFFFAOYSA-N 0.000 description 1
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- JTJMJGYZQZDUJJ-UHFFFAOYSA-N phencyclidine Chemical compound C1CCCCN1C1(C=2C=CC=CC=2)CCCCC1 JTJMJGYZQZDUJJ-UHFFFAOYSA-N 0.000 description 1
- XEBWQGVWTUSTLN-UHFFFAOYSA-M phenylmercury acetate Chemical compound CC(=O)O[Hg]C1=CC=CC=C1 XEBWQGVWTUSTLN-UHFFFAOYSA-M 0.000 description 1
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- TZLVRPLSVNESQC-UHFFFAOYSA-N potassium azide Chemical compound [K+].[N-]=[N+]=[N-] TZLVRPLSVNESQC-UHFFFAOYSA-N 0.000 description 1
- GKKCIDNWFBPDBW-UHFFFAOYSA-M potassium cyanate Chemical compound [K]OC#N GKKCIDNWFBPDBW-UHFFFAOYSA-M 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- ISEUFVQQFVOBCY-UHFFFAOYSA-N prometon Chemical compound COC1=NC(NC(C)C)=NC(NC(C)C)=N1 ISEUFVQQFVOBCY-UHFFFAOYSA-N 0.000 description 1
- AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 1
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 235000009736 ragweed Nutrition 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 235000003513 sheep sorrel Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- HKAMKLBXTLTVCN-UHFFFAOYSA-N simeton Chemical compound CCNC1=NC(NCC)=NC(OC)=N1 HKAMKLBXTLTVCN-UHFFFAOYSA-N 0.000 description 1
- 201000010153 skin papilloma Diseases 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- NTOCDDPMRUNYHP-UHFFFAOYSA-M sodium;2-(2,4,5-trichlorophenoxy)ethyl sulfate Chemical compound [Na+].[O-]S(=O)(=O)OCCOC1=CC(Cl)=C(Cl)C=C1Cl NTOCDDPMRUNYHP-UHFFFAOYSA-M 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 235000005765 wild carrot Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/27—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
- C07C205/35—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/36—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system
- C07C205/37—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton to carbon atoms of the same non-condensed six-membered aromatic ring or to carbon atoms of six-membered aromatic rings being part of the same condensed ring system the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/14—Radicals substituted by nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D307/52—Radicals substituted by nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/391,088 US4404018A (en) | 1982-06-23 | 1982-06-23 | Furfuryl amides of phenoxyphenoxyalkanoic acids and herbicidal use |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO832269L true NO832269L (no) | 1983-12-27 |
Family
ID=23545184
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO832269A NO832269L (no) | 1982-06-23 | 1983-06-22 | Furfurylamider av fenoksy-fenoksy-alkansyrer. |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US4404018A (da) |
| JP (1) | JPS5910576A (da) |
| KR (1) | KR860001029B1 (da) |
| AU (1) | AU554518B2 (da) |
| BE (1) | BE897097A (da) |
| CA (1) | CA1177837A (da) |
| CH (1) | CH653677A5 (da) |
| DD (1) | DD218827A5 (da) |
| DE (1) | DE3322261A1 (da) |
| DK (1) | DK288383A (da) |
| ES (1) | ES523047A0 (da) |
| FR (1) | FR2529205B1 (da) |
| GB (1) | GB2122187B (da) |
| GR (1) | GR78314B (da) |
| IL (1) | IL68372A0 (da) |
| IN (1) | IN159372B (da) |
| IT (1) | IT1170401B (da) |
| NL (1) | NL8301753A (da) |
| NO (1) | NO832269L (da) |
| NZ (1) | NZ203796A (da) |
| PH (1) | PH17521A (da) |
| RO (1) | RO87255A (da) |
| SE (1) | SE8303427L (da) |
| YU (1) | YU92983A (da) |
| ZA (1) | ZA832636B (da) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4402729A (en) * | 1982-05-07 | 1983-09-06 | Velsicol Chemical Corporation | Heterocyclic amides of phenoxyphenoxyalkanoic acids |
| AR057455A1 (es) * | 2005-07-22 | 2007-12-05 | Merck & Co Inc | Inhibidores de la transcriptasa reversa de vih y composicion farmaceutica |
| WO2012061698A2 (en) * | 2010-11-05 | 2012-05-10 | Senomyx, Inc. | Compounds useful as modulators of trpm8 |
| JP6865743B2 (ja) | 2015-10-01 | 2021-04-28 | フィルメニッヒ インコーポレイテッドＦｉｒｍｅｎｉｃｈ Ｉｎｃｏｒｐｏｒａｔｅｄ | Ｔｒｐｍ８の活性調節因子として有用な化合物 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3326942A (en) * | 1963-10-22 | 1967-06-20 | Plant Products Corp | Herbicidal substituted phenoxy acylamides |
| DE2850902A1 (de) * | 1978-11-24 | 1980-06-12 | Hoechst Ag | Neue phenoxy-phenoxi-propionsaeureamide und ihre verwendung als herbizide |
| AU6651581A (en) * | 1980-02-01 | 1981-08-06 | Rhone-Poulenc, Inc. | 2-nitro-(substituted phenoxy) benzoyl derivatives as herbicides |
-
1982
- 1982-06-23 US US06/391,088 patent/US4404018A/en not_active Expired - Fee Related
-
1983
- 1983-04-06 IN IN228/DEL/83A patent/IN159372B/en unknown
- 1983-04-06 NZ NZ203796A patent/NZ203796A/en unknown
- 1983-04-08 CA CA000425524A patent/CA1177837A/en not_active Expired
- 1983-04-13 IL IL68372A patent/IL68372A0/xx unknown
- 1983-04-14 ZA ZA832636A patent/ZA832636B/xx unknown
- 1983-04-22 GB GB08310914A patent/GB2122187B/en not_active Expired
- 1983-04-25 YU YU00929/83A patent/YU92983A/xx unknown
- 1983-04-27 CH CH2259/83A patent/CH653677A5/de not_active IP Right Cessation
- 1983-05-02 PH PH28838A patent/PH17521A/en unknown
- 1983-05-17 NL NL8301753A patent/NL8301753A/nl not_active Application Discontinuation
- 1983-05-20 FR FR8308405A patent/FR2529205B1/fr not_active Expired
- 1983-05-24 KR KR1019830002279A patent/KR860001029B1/ko active
- 1983-05-31 DD DD83251541A patent/DD218827A5/de unknown
- 1983-06-07 ES ES523047A patent/ES523047A0/es active Granted
- 1983-06-13 JP JP58105633A patent/JPS5910576A/ja active Pending
- 1983-06-13 IT IT48492/83A patent/IT1170401B/it active
- 1983-06-15 SE SE8303427A patent/SE8303427L/xx not_active Application Discontinuation
- 1983-06-20 BE BE0/211039A patent/BE897097A/fr not_active IP Right Cessation
- 1983-06-20 GR GR71727A patent/GR78314B/el unknown
- 1983-06-21 DE DE19833322261 patent/DE3322261A1/de not_active Withdrawn
- 1983-06-21 RO RO83111366A patent/RO87255A/ro unknown
- 1983-06-22 NO NO832269A patent/NO832269L/no unknown
- 1983-06-22 AU AU16148/83A patent/AU554518B2/en not_active Ceased
- 1983-06-22 DK DK288383A patent/DK288383A/da not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| IN159372B (da) | 1987-05-09 |
| IT8348492A0 (it) | 1983-06-13 |
| IL68372A0 (en) | 1983-07-31 |
| ES8500255A1 (es) | 1984-10-01 |
| KR840005121A (ko) | 1984-11-03 |
| JPS5910576A (ja) | 1984-01-20 |
| ES523047A0 (es) | 1984-10-01 |
| FR2529205A1 (fr) | 1983-12-30 |
| BE897097A (fr) | 1983-10-17 |
| US4404018A (en) | 1983-09-13 |
| KR860001029B1 (ko) | 1986-07-28 |
| DD218827A5 (de) | 1985-02-20 |
| YU92983A (en) | 1986-02-28 |
| GR78314B (da) | 1984-09-26 |
| CH653677A5 (de) | 1986-01-15 |
| NZ203796A (en) | 1985-04-30 |
| ZA832636B (en) | 1983-12-28 |
| DK288383A (da) | 1983-12-24 |
| AU554518B2 (en) | 1986-08-21 |
| FR2529205B1 (fr) | 1986-12-26 |
| GB2122187A (en) | 1984-01-11 |
| PH17521A (en) | 1984-09-13 |
| DK288383D0 (da) | 1983-06-22 |
| GB8310914D0 (en) | 1983-05-25 |
| IT1170401B (it) | 1987-06-03 |
| DE3322261A1 (de) | 1983-12-29 |
| NL8301753A (nl) | 1984-01-16 |
| SE8303427L (sv) | 1983-12-24 |
| CA1177837A (en) | 1984-11-13 |
| SE8303427D0 (sv) | 1983-06-15 |
| AU1614883A (en) | 1984-01-05 |
| GB2122187B (en) | 1985-11-06 |
| RO87255A (ro) | 1985-11-30 |
| RO87255B (ro) | 1985-10-31 |
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