CA1273921A - 3-aryl-5, 6-dihydro-1, 4, 2-oxathiazines and their oxides - Google Patents
3-aryl-5, 6-dihydro-1, 4, 2-oxathiazines and their oxidesInfo
- Publication number
- CA1273921A CA1273921A CA000437514A CA437514A CA1273921A CA 1273921 A CA1273921 A CA 1273921A CA 000437514 A CA000437514 A CA 000437514A CA 437514 A CA437514 A CA 437514A CA 1273921 A CA1273921 A CA 1273921A
- Authority
- CA
- Canada
- Prior art keywords
- compound
- phenyl
- hydrogen
- phenyl substituted
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 claims abstract description 96
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 94
- -1 tetrahydropyranyloxy furanyl phenoxy furanyl Chemical group 0.000 claims abstract description 62
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 49
- 239000001257 hydrogen Substances 0.000 claims abstract description 49
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 40
- 238000000034 method Methods 0.000 claims abstract description 36
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 32
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 28
- 125000001544 thienyl group Chemical group 0.000 claims abstract description 18
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 17
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 15
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 13
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims abstract description 11
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract description 6
- 239000002837 defoliant Substances 0.000 claims abstract description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 3
- 241000196324 Embryophyta Species 0.000 claims description 64
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 33
- 125000002541 furyl group Chemical group 0.000 claims description 29
- 229910052801 chlorine Inorganic materials 0.000 claims description 19
- 239000002904 solvent Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 16
- 241000233866 Fungi Species 0.000 claims description 15
- 230000002363 herbicidal effect Effects 0.000 claims description 15
- 229910052794 bromium Inorganic materials 0.000 claims description 12
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- KPCZJLGGXRGYIE-UHFFFAOYSA-N [C]1=CC=CN=C1 Chemical group [C]1=CC=CN=C1 KPCZJLGGXRGYIE-UHFFFAOYSA-N 0.000 claims description 10
- 239000002585 base Substances 0.000 claims description 10
- 125000001475 halogen functional group Chemical group 0.000 claims description 10
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 8
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 8
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 claims description 8
- 230000000855 fungicidal effect Effects 0.000 claims description 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
- 125000001624 naphthyl group Chemical group 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 5
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 125000006518 morpholino carbonyl group Chemical group [H]C1([H])OC([H])([H])C([H])([H])N(C(*)=O)C1([H])[H] 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 3
- 239000000528 plant desiccant Substances 0.000 claims description 3
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 claims description 2
- 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 2
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 2
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims 5
- 230000001276 controlling effect Effects 0.000 claims 3
- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 claims 3
- 125000005843 halogen group Chemical group 0.000 claims 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 2
- MGNKCLCKFJFDOU-UHFFFAOYSA-N NSO Chemical compound NSO MGNKCLCKFJFDOU-UHFFFAOYSA-N 0.000 claims 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims 1
- 230000008635 plant growth Effects 0.000 claims 1
- 230000001105 regulatory effect Effects 0.000 claims 1
- 239000004009 herbicide Substances 0.000 abstract description 17
- 239000000417 fungicide Substances 0.000 abstract description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract description 3
- 230000003115 biocidal effect Effects 0.000 abstract description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 description 56
- 239000000126 substance Substances 0.000 description 45
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 42
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 41
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 32
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
- 201000010099 disease Diseases 0.000 description 24
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 24
- 239000000243 solution Substances 0.000 description 19
- 239000004094 surface-active agent Substances 0.000 description 18
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- 239000000725 suspension Substances 0.000 description 16
- 229920000742 Cotton Polymers 0.000 description 15
- 239000007787 solid Substances 0.000 description 15
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 14
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 14
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 14
- 229940086542 triethylamine Drugs 0.000 description 14
- 239000004480 active ingredient Substances 0.000 description 13
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 12
- 239000007921 spray Substances 0.000 description 12
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 11
- 244000237956 Amaranthus retroflexus Species 0.000 description 11
- 230000035613 defoliation Effects 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
- 238000009472 formulation Methods 0.000 description 10
- 240000006995 Abutilon theophrasti Species 0.000 description 9
- 235000001602 Digitaria X umfolozi Nutrition 0.000 description 9
- 240000003176 Digitaria ciliaris Species 0.000 description 9
- 235000017898 Digitaria ciliaris Nutrition 0.000 description 9
- 235000005476 Digitaria cruciata Nutrition 0.000 description 9
- 235000006830 Digitaria didactyla Nutrition 0.000 description 9
- 235000005804 Digitaria eriantha ssp. eriantha Nutrition 0.000 description 9
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 9
- 235000014716 Eleusine indica Nutrition 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- AZHVQJLDOFKHPZ-UHFFFAOYSA-N oxathiazine Chemical class O1SN=CC=C1 AZHVQJLDOFKHPZ-UHFFFAOYSA-N 0.000 description 9
- QXMAXBCUOKUJJZ-UHFFFAOYSA-N 3-(4-chlorophenyl)-5,6-dihydro-1,4,2-oxathiazine Chemical compound C1=CC(Cl)=CC=C1C1=NOCCS1 QXMAXBCUOKUJJZ-UHFFFAOYSA-N 0.000 description 8
- 235000004135 Amaranthus viridis Nutrition 0.000 description 8
- 235000009344 Chenopodium album Nutrition 0.000 description 8
- 235000005484 Chenopodium berlandieri Nutrition 0.000 description 8
- 235000009332 Chenopodium rubrum Nutrition 0.000 description 8
- 235000010469 Glycine max Nutrition 0.000 description 8
- 244000068988 Glycine max Species 0.000 description 8
- 238000007792 addition Methods 0.000 description 8
- 239000002270 dispersing agent Substances 0.000 description 8
- FMYSHKHSQFXYRS-UHFFFAOYSA-N 1,4,2-oxathiazine Chemical class O1C=CSC=N1 FMYSHKHSQFXYRS-UHFFFAOYSA-N 0.000 description 7
- 235000003403 Limnocharis flava Nutrition 0.000 description 7
- 238000003306 harvesting Methods 0.000 description 7
- 208000015181 infectious disease Diseases 0.000 description 7
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 6
- MDFSPNRAZLWJCB-UHFFFAOYSA-N 3-(2-chlorophenyl)-5,6-dihydro-1,4,2-oxathiazine Chemical compound ClC1=CC=CC=C1C1=NOCCS1 MDFSPNRAZLWJCB-UHFFFAOYSA-N 0.000 description 6
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 6
- 240000001592 Amaranthus caudatus Species 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 150000002431 hydrogen Chemical group 0.000 description 6
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 6
- 235000019341 magnesium sulphate Nutrition 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- WTFVNJUBLNKGGZ-UHFFFAOYSA-N 3-(3-fluorophenyl)-5,6-dihydro-1,4,2-oxathiazine Chemical compound FC1=CC=CC(C=2SCCON=2)=C1 WTFVNJUBLNKGGZ-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
- 239000000969 carrier Substances 0.000 description 5
- 239000012153 distilled water Substances 0.000 description 5
- 230000003902 lesion Effects 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- ITHKUADHDKZENI-UHFFFAOYSA-N 2-chloroethanethiol Chemical compound SCCCl ITHKUADHDKZENI-UHFFFAOYSA-N 0.000 description 4
- JMBBLMILRMYPGK-UHFFFAOYSA-N 3-(3-chlorophenyl)-5,6-dihydro-1,4,2-oxathiazine Chemical compound ClC1=CC=CC(C=2SCCON=2)=C1 JMBBLMILRMYPGK-UHFFFAOYSA-N 0.000 description 4
- CFLWOXCTTSFMSX-UHFFFAOYSA-N 3-pyridin-4-yl-5,6-dihydro-1,4,2-oxathiazine Chemical compound O1CCSC(C=2C=CN=CC=2)=N1 CFLWOXCTTSFMSX-UHFFFAOYSA-N 0.000 description 4
- 244000025254 Cannabis sativa Species 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 244000058871 Echinochloa crus-galli Species 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 229920001213 Polysorbate 20 Polymers 0.000 description 4
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- 235000002248 Setaria viridis Nutrition 0.000 description 4
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- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 229940073584 methylene chloride Drugs 0.000 description 4
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 4
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
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- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- MTGXUZCZZQPRHK-UHFFFAOYSA-N 3-thiophen-2-yl-5,6-dihydro-1,4,2-oxathiazine Chemical compound O1CCSC(C=2SC=CC=2)=N1 MTGXUZCZZQPRHK-UHFFFAOYSA-N 0.000 description 3
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
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- PPNAETJSOVRPEY-UHFFFAOYSA-N ethyl 4-(5,6-dihydro-1,4,2-oxathiazin-3-yl)benzoate Chemical compound C1=CC(C(=O)OCC)=CC=C1C1=NOCCS1 PPNAETJSOVRPEY-UHFFFAOYSA-N 0.000 description 3
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 3
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- 239000004563 wettable powder Substances 0.000 description 3
- YVPILVVQLFIONM-UHFFFAOYSA-N 2-chloroethyl 2-chloro-n-hydroxybenzenecarboximidothioate Chemical compound ClCCSC(=NO)C1=CC=CC=C1Cl YVPILVVQLFIONM-UHFFFAOYSA-N 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- MWKLMPNZCHVCJY-UHFFFAOYSA-N 3-(2,6-dichlorophenyl)-5,6-dihydro-1,4,2-oxathiazine Chemical compound ClC1=CC=CC(Cl)=C1C1=NOCCS1 MWKLMPNZCHVCJY-UHFFFAOYSA-N 0.000 description 2
- PTTCZVCORVHPHU-UHFFFAOYSA-N 3-(furan-2-yl)-5,6-dihydro-1,4,2-oxathiazine Chemical compound O1CCSC(C=2OC=CC=2)=N1 PTTCZVCORVHPHU-UHFFFAOYSA-N 0.000 description 2
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- 125000006539 C12 alkyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
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- KFYMDOOXSJOTNI-FLIBITNWSA-N (nz)-n-(6-fluoro-2,3-dihydrothiochromen-4-ylidene)hydroxylamine Chemical compound C1=C(F)C=C2C(=N/O)\CCSC2=C1 KFYMDOOXSJOTNI-FLIBITNWSA-N 0.000 description 1
- ZFFMHBULJWGCKI-UITAMQMPSA-N (nz)-n-[(3-fluorophenyl)methylidene]hydroxylamine Chemical compound O\N=C/C1=CC=CC(F)=C1 ZFFMHBULJWGCKI-UITAMQMPSA-N 0.000 description 1
- XFNJYAKDBJUJAJ-UHFFFAOYSA-N 1,2-dibromopropane Chemical compound CC(Br)CBr XFNJYAKDBJUJAJ-UHFFFAOYSA-N 0.000 description 1
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- BZJCQLOKQOJURT-UHFFFAOYSA-N 2-chloroethyl 3-fluoro-n-hydroxybenzenecarboximidothioate Chemical compound ClCCSC(=NO)C1=CC=CC(F)=C1 BZJCQLOKQOJURT-UHFFFAOYSA-N 0.000 description 1
- VHPDZGGVYZRVSV-UHFFFAOYSA-N 2-chloroethyl 4-chloro-n-hydroxybenzenecarboximidothioate Chemical compound ClCCSC(=NO)C1=CC=C(Cl)C=C1 VHPDZGGVYZRVSV-UHFFFAOYSA-N 0.000 description 1
- QVLQFSAHRMARCQ-UHFFFAOYSA-N 2-chloroethyl N-hydroxypyridine-4-carboximidothioate Chemical compound ON=C(SCCCl)C1=CC=NC=C1 QVLQFSAHRMARCQ-UHFFFAOYSA-N 0.000 description 1
- ZMMAZZPEBLRILP-UHFFFAOYSA-N 2-chloroethyl n-hydroxybenzenecarboximidothioate Chemical class ClCCSC(=NO)C1=CC=CC=C1 ZMMAZZPEBLRILP-UHFFFAOYSA-N 0.000 description 1
- MDLKFPDOGLWJFQ-UHFFFAOYSA-N 2-hydroxybenzenecarboximidoyl chloride Chemical compound Oc1ccccc1C(Cl)=N MDLKFPDOGLWJFQ-UHFFFAOYSA-N 0.000 description 1
- LLIKRGYMSLBACA-UHFFFAOYSA-N 3-(2,6-dichlorophenyl)-5,6-dihydro-1,4,2-oxathiazine 4,4-dioxide Chemical compound ClC1=CC=CC(Cl)=C1C1=NOCCS1(=O)=O LLIKRGYMSLBACA-UHFFFAOYSA-N 0.000 description 1
- CUXZLTKEDZEXJX-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5,6-dihydro-1,4,2-oxathiazine Chemical compound ClC1=CC(Cl)=CC(C=2SCCON=2)=C1 CUXZLTKEDZEXJX-UHFFFAOYSA-N 0.000 description 1
- IUJHWOALNLCMFU-UHFFFAOYSA-N 3-(3-fluorophenyl)-5,6-dihydro-1,4,2-oxathiazine 4-oxide Chemical compound FC1=CC=CC(C=2S(CCON=2)=O)=C1 IUJHWOALNLCMFU-UHFFFAOYSA-N 0.000 description 1
- DXPBAIHCKYJQTE-UHFFFAOYSA-N 3-(3-nitrophenyl)-5,6-dihydro-1,4,2-oxathiazine Chemical compound [O-][N+](=O)C1=CC=CC(C=2SCCON=2)=C1 DXPBAIHCKYJQTE-UHFFFAOYSA-N 0.000 description 1
- CAEBCYZXPZVDAT-UHFFFAOYSA-N 3-(4-bromophenyl)-5,6-dihydro-1,4,2-oxathiazine Chemical compound C1=CC(Br)=CC=C1C1=NOCCS1 CAEBCYZXPZVDAT-UHFFFAOYSA-N 0.000 description 1
- RKHCYJUGSFIRMY-UHFFFAOYSA-N 3-(5,6-dihydro-1,4,2-oxathiazin-3-yl)-n-phenylbenzamide Chemical compound C=1C=CC(C=2SCCON=2)=CC=1C(=O)NC1=CC=CC=C1 RKHCYJUGSFIRMY-UHFFFAOYSA-N 0.000 description 1
- IGBHWHNREWWSMY-UHFFFAOYSA-N 3-(5,6-dihydro-1,4,2-oxathiazin-3-yl)benzoic acid Chemical compound OC(=O)C1=CC=CC(C=2SCCON=2)=C1 IGBHWHNREWWSMY-UHFFFAOYSA-N 0.000 description 1
- XPYQFIISZQCINN-QVXDJYSKSA-N 4-amino-1-[(2r,3e,4s,5r)-3-(fluoromethylidene)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidin-2-one;hydrate Chemical compound O.O=C1N=C(N)C=CN1[C@H]1C(=C/F)/[C@H](O)[C@@H](CO)O1 XPYQFIISZQCINN-QVXDJYSKSA-N 0.000 description 1
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical class CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 241001530056 Athelia rolfsii Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
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- DRSHXJFUUPIBHX-UHFFFAOYSA-N COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 Chemical compound COc1ccc(cc1)N1N=CC2C=NC(Nc3cc(OC)c(OC)c(OCCCN4CCN(C)CC4)c3)=NC12 DRSHXJFUUPIBHX-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241001157813 Cercospora Species 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- 241000208296 Datura Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
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- 241000223221 Fusarium oxysporum Species 0.000 description 1
- 241000208818 Helianthus Species 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 241001330975 Magnaporthe oryzae Species 0.000 description 1
- OFYLBLSSPQTTHT-UHFFFAOYSA-N N-(pyridin-4-ylmethylidene)hydroxylamine Chemical compound ON=CC1=CC=NC=C1 OFYLBLSSPQTTHT-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 241000209094 Oryza Species 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 241000233614 Phytophthora Species 0.000 description 1
- 241000209504 Poaceae Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 241000233639 Pythium Species 0.000 description 1
- 241001385948 Pythium sp. Species 0.000 description 1
- 241001558929 Sclerotium <basidiomycota> Species 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 235000018694 Solanum laxum Nutrition 0.000 description 1
- 235000000305 Solanum wendlandii Nutrition 0.000 description 1
- 240000004488 Solanum wendlandii Species 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- ZDZHCHYQNPQSGG-UHFFFAOYSA-N binaphthyl group Chemical class C1(=CC=CC2=CC=CC=C12)C1=CC=CC2=CC=CC=C12 ZDZHCHYQNPQSGG-UHFFFAOYSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 239000011436 cob Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 125000005879 dioxolanyl group Chemical group 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 244000013123 dwarf bean Species 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
- FLUBFQHBYAZHON-UHFFFAOYSA-N ethyl 3-(trifluoromethyl)benzenecarbodithioate Chemical compound CCSC(=S)C1=CC=CC(C(F)(F)F)=C1 FLUBFQHBYAZHON-UHFFFAOYSA-N 0.000 description 1
- ZURPSWQDKUBGHU-UHFFFAOYSA-N ethyl 4-bromobenzenecarbodithioate Chemical compound CCSC(=S)C1=CC=C(Br)C=C1 ZURPSWQDKUBGHU-UHFFFAOYSA-N 0.000 description 1
- PTQBHRKOKUYMRC-UHFFFAOYSA-N ethyl 4-methylsulfanylcarbothioylbenzoate Chemical compound CCOC(=O)C1=CC=C(C(=S)SC)C=C1 PTQBHRKOKUYMRC-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000035558 fertility Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000004345 fruit ripening Effects 0.000 description 1
- 244000053095 fungal pathogen Species 0.000 description 1
- 230000002464 fungitoxic effect Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- AVUAQZWZYNFGQX-UHFFFAOYSA-N methyl 3-nitrobenzenecarbodithioate Chemical compound CSC(=S)C1=CC=CC([N+]([O-])=O)=C1 AVUAQZWZYNFGQX-UHFFFAOYSA-N 0.000 description 1
- VVUHENBZWKSXCS-UHFFFAOYSA-N methyl furan-2-carbodithioate Chemical compound CSC(=S)C1=CC=CO1 VVUHENBZWKSXCS-UHFFFAOYSA-N 0.000 description 1
- QTFGJYVLAVUFIX-UHFFFAOYSA-N methyl thiophene-2-carbodithioate Chemical compound CSC(=S)C1=CC=CS1 QTFGJYVLAVUFIX-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000010813 municipal solid waste Substances 0.000 description 1
- FDURJBZDDIIFAL-UHFFFAOYSA-N n-(5,6-dimethyl-3-phenyl-5h-1,4,2-oxathiazin-6-yl)acetamide Chemical class O1C(NC(C)=O)(C)C(C)SC(C=2C=CC=CC=2)=N1 FDURJBZDDIIFAL-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- DHHVAGZRUROJKS-UHFFFAOYSA-N phentermine Chemical compound CC(C)(N)CC1=CC=CC=C1 DHHVAGZRUROJKS-UHFFFAOYSA-N 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
- 230000008654 plant damage Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000009290 primary effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000004016 soil organic matter Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- IXZDIALLLMRYOU-UHFFFAOYSA-N tert-butyl hypochlorite Chemical compound CC(C)(C)OCl IXZDIALLLMRYOU-UHFFFAOYSA-N 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D419/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms
- C07D419/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D419/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D291/00—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms
- C07D291/02—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms not condensed with other rings
- C07D291/06—Six-membered rings
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C07C327/58—Derivatives of thiocarboxylic acids, the doubly-bound oxygen atoms being replaced by nitrogen atoms, e.g. imino-thio ethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D419/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms
- C07D419/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D419/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen, oxygen, and sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US42573982A | 1982-09-28 | 1982-09-28 | |
| US425,739 | 1982-09-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1273921A true CA1273921A (en) | 1990-09-11 |
Family
ID=23687821
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000437514A Expired CA1273921A (en) | 1982-09-28 | 1983-09-26 | 3-aryl-5, 6-dihydro-1, 4, 2-oxathiazines and their oxides |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP0104940A1 (OSRAM) |
| JP (1) | JPS5980670A (OSRAM) |
| KR (1) | KR840006229A (OSRAM) |
| AU (1) | AU544881B2 (OSRAM) |
| BR (1) | BR8305330A (OSRAM) |
| CA (1) | CA1273921A (OSRAM) |
| DD (1) | DD215781A5 (OSRAM) |
| ES (1) | ES8507528A1 (OSRAM) |
| GB (1) | GB2127817B (OSRAM) |
| GR (1) | GR78990B (OSRAM) |
| IL (1) | IL69839A0 (OSRAM) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CZ286710B6 (en) * | 1993-08-24 | 2000-06-14 | Janssen Pharmaceutica Nv | Method of suppressing bacteria and contaminating organisms and coating compositions |
| MX9406411A (es) * | 1993-08-24 | 1997-08-30 | Uniroyal Chem Co Inc | Oxatiazinas conservadoras de madera. |
| SK107597A3 (en) | 1995-02-13 | 1998-02-04 | Bayer Ag | Fungicidal aza-heterocycloalkenes, producing method thereof, agents for killing the pests containing the same, method of killing the pests and use said compounds |
| BR9811939A (pt) * | 1997-08-14 | 2000-09-05 | Bayer Ag | Metoximinometiloxadiazinas como pesticidas |
| GB9826245D0 (en) * | 1998-11-30 | 1999-01-20 | Hickson Int Plc | Wood preserative formulations |
| WO2011039276A1 (de) | 2009-10-01 | 2011-04-07 | Bayer Cropscience Ag | Oxathiazinyl-(het)arylsulfonylharnstoffe, verfahren und zwischenprodukte zu ihrer herstellung und ihre verwendung als planzenschutzmittel und pflaznenwachstumsregulatoren |
-
1983
- 1983-09-26 CA CA000437514A patent/CA1273921A/en not_active Expired
- 1983-09-27 IL IL69839A patent/IL69839A0/xx unknown
- 1983-09-27 GB GB08325754A patent/GB2127817B/en not_active Expired
- 1983-09-27 AU AU19618/83A patent/AU544881B2/en not_active Ceased
- 1983-09-27 EP EP83305783A patent/EP0104940A1/en not_active Withdrawn
- 1983-09-27 ES ES525994A patent/ES8507528A1/es not_active Expired
- 1983-09-27 GR GR72548A patent/GR78990B/el unknown
- 1983-09-28 BR BR8305330A patent/BR8305330A/pt unknown
- 1983-09-28 KR KR1019830004570A patent/KR840006229A/ko not_active Withdrawn
- 1983-09-28 DD DD83255193A patent/DD215781A5/de unknown
- 1983-09-28 JP JP58180109A patent/JPS5980670A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5980670A (ja) | 1984-05-10 |
| BR8305330A (pt) | 1984-05-08 |
| DD215781A5 (de) | 1984-11-21 |
| ES525994A0 (es) | 1985-09-16 |
| IL69839A0 (en) | 1983-12-30 |
| AU544881B2 (en) | 1985-06-20 |
| GB2127817A (en) | 1984-04-18 |
| ES8507528A1 (es) | 1985-09-16 |
| GB2127817B (en) | 1985-12-18 |
| KR840006229A (ko) | 1984-11-22 |
| AU1961883A (en) | 1984-04-05 |
| GB8325754D0 (en) | 1983-10-26 |
| GR78990B (OSRAM) | 1984-10-02 |
| EP0104940A1 (en) | 1984-04-04 |
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