HRP960167A2 - New hydroximic acid derivatives - Google Patents
New hydroximic acid derivatives Download PDFInfo
- Publication number
- HRP960167A2 HRP960167A2 HRPTC/IB96/00276A HRP960167A HRP960167A2 HR P960167 A2 HRP960167 A2 HR P960167A2 HR P960167 A HRP960167 A HR P960167A HR P960167 A2 HRP960167 A2 HR P960167A2
- Authority
- HR
- Croatia
- Prior art keywords
- compound
- group
- formula
- hydrogen
- methyl
- Prior art date
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- 239000002253 acid Substances 0.000 title claims description 30
- 150000001875 compounds Chemical class 0.000 claims description 136
- 238000000034 method Methods 0.000 claims description 50
- 238000002360 preparation method Methods 0.000 claims description 41
- 239000002904 solvent Substances 0.000 claims description 34
- -1 mercapto, nitro, thiocyano Chemical group 0.000 claims description 32
- 238000006243 chemical reaction Methods 0.000 claims description 30
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 239000013543 active substance Substances 0.000 claims description 21
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 21
- 239000001257 hydrogen Substances 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- 125000001188 haloalkyl group Chemical group 0.000 claims description 15
- 235000013339 cereals Nutrition 0.000 claims description 14
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims description 12
- 125000003545 alkoxy group Chemical group 0.000 claims description 12
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- 208000031888 Mycoses Diseases 0.000 claims description 10
- 239000000575 pesticide Substances 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 125000000304 alkynyl group Chemical group 0.000 claims description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- 230000000855 fungicidal effect Effects 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 5
- 238000009835 boiling Methods 0.000 claims description 5
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 5
- 125000005347 halocycloalkyl group Chemical group 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 239000011593 sulfur Substances 0.000 claims description 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 239000012442 inert solvent Substances 0.000 claims description 4
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- 125000004663 dialkyl amino group Chemical group 0.000 claims description 3
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- 125000004442 acylamino group Chemical group 0.000 claims description 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 2
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- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
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- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 2
- 125000005133 alkynyloxy group Chemical group 0.000 claims description 2
- 125000005109 alkynylthio group Chemical group 0.000 claims description 2
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 claims description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 2
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 claims description 2
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- 125000004995 haloalkylthio group Chemical group 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004438 haloalkoxy group Chemical group 0.000 claims 2
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- 125000005159 cyanoalkoxy group Chemical group 0.000 claims 1
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- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- JBSLOWBPDRZSMB-FPLPWBNLSA-N dibutyl (z)-but-2-enedioate Chemical compound CCCCOC(=O)\C=C/C(=O)OCCCC JBSLOWBPDRZSMB-FPLPWBNLSA-N 0.000 description 1
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 235000021186 dishes Nutrition 0.000 description 1
- YHAIUSTWZPMYGG-UHFFFAOYSA-L disodium;2,2-dioctyl-3-sulfobutanedioate Chemical compound [Na+].[Na+].CCCCCCCCC(C([O-])=O)(C(C([O-])=O)S(O)(=O)=O)CCCCCCCC YHAIUSTWZPMYGG-UHFFFAOYSA-L 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
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- 241001233061 earthworms Species 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 244000037666 field crops Species 0.000 description 1
- 235000019688 fish Nutrition 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000012055 fruits and vegetables Nutrition 0.000 description 1
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- 229920000159 gelatin Polymers 0.000 description 1
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- 235000011852 gelatine desserts Nutrition 0.000 description 1
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- 230000012010 growth Effects 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
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- 210000004209 hair Anatomy 0.000 description 1
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 description 1
- 150000005171 halobenzenes Chemical class 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
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- 229940071826 hydroxyethyl cellulose Drugs 0.000 description 1
- 150000002443 hydroxylamines Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 125000005928 isopropyloxycarbonyl group Chemical group [H]C([H])([H])C([H])(OC(*)=O)C([H])([H])[H] 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- AHGSMGJSDRLMNU-UHFFFAOYSA-N methyl 2-[2-[(c-ethyl-n-phenylmethoxycarbonimidoyl)oxymethyl]phenyl]-3-methoxyprop-2-enoate Chemical compound C=1C=CC=CC=1CON=C(CC)OCC1=CC=CC=C1C(=COC)C(=O)OC AHGSMGJSDRLMNU-UHFFFAOYSA-N 0.000 description 1
- YEMBVPQSORWGRO-UHFFFAOYSA-N methyl 3-methoxy-2-[2-[(c-methyl-n-phenylmethoxycarbonimidoyl)oxymethyl]phenyl]prop-2-enoate Chemical compound COC=C(C(=O)OC)C1=CC=CC=C1COC(C)=NOCC1=CC=CC=C1 YEMBVPQSORWGRO-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229960002900 methylcellulose Drugs 0.000 description 1
- 229940073584 methylene chloride Drugs 0.000 description 1
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-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
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- CIYAOKYMIFEWAU-UHFFFAOYSA-N n-phenylmethoxypropanethioamide Chemical compound CCC(=S)NOCC1=CC=CC=C1 CIYAOKYMIFEWAU-UHFFFAOYSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 235000014571 nuts Nutrition 0.000 description 1
- XYEOALKITRFCJJ-UHFFFAOYSA-N o-benzylhydroxylamine Chemical compound NOCC1=CC=CC=C1 XYEOALKITRFCJJ-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- VSIIXMUUUJUKCM-UHFFFAOYSA-D pentacalcium;fluoride;triphosphate Chemical compound [F-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O VSIIXMUUUJUKCM-UHFFFAOYSA-D 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- DDBREPKUVSBGFI-UHFFFAOYSA-N phenobarbital Chemical compound C=1C=CC=CC=1C1(CC)C(=O)NC(=O)NC1=O DDBREPKUVSBGFI-UHFFFAOYSA-N 0.000 description 1
- CNMBRKNJGAKOIO-UHFFFAOYSA-N phenyl 2-methoxyiminoacetate Chemical compound CON=CC(=O)OC1=CC=CC=C1 CNMBRKNJGAKOIO-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 description 1
- 230000003032 phytopathogenic effect Effects 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229940068984 polyvinyl alcohol Drugs 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical compound [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 description 1
- 229910000105 potassium hydride Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 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 1
- 230000005855 radiation Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 239000004460 silage Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- KNOGXLBAOQDKTG-UHFFFAOYSA-M sodium;2-ethylhexane-1-sulfonate Chemical compound [Na+].CCCCC(CC)CS([O-])(=O)=O KNOGXLBAOQDKTG-UHFFFAOYSA-M 0.000 description 1
- FGDMJJQHQDFUCP-UHFFFAOYSA-M sodium;2-propan-2-ylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=CC2=C(S([O-])(=O)=O)C(C(C)C)=CC=C21 FGDMJJQHQDFUCP-UHFFFAOYSA-M 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 235000013616 tea Nutrition 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 239000013598 vector Substances 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
- 230000000007 visual effect Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000010457 zeolite 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
- C07C259/06—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
- C07C259/08—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
- C07C259/10—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to carbon atoms of six-membered aromatic rings
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C07C327/60—Thiocarboxylic acids having sulfur atoms of thiocarboxyl groups further doubly-bound to oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9073395 | 1995-04-17 | ||
| EP9502984 | 1995-07-27 | ||
| JP7194670A JPH093031A (ja) | 1995-04-17 | 1995-07-31 | ヒドロキサム酸誘導体並びにそれを含有する農園芸用殺菌剤 |
| IB9600276 | 1996-01-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HRP960167A2 true HRP960167A2 (en) | 1997-10-31 |
Family
ID=26432174
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HRPTC/IB96/00276A HRP960167A2 (en) | 1995-04-17 | 1996-04-12 | New hydroximic acid derivatives |
Country Status (23)
| Country | Link |
|---|---|
| US (2) | US5919825A (fr) |
| EP (1) | EP0821667A1 (fr) |
| JP (2) | JPH093031A (fr) |
| KR (1) | KR19990007856A (fr) |
| AP (1) | AP9701140A0 (fr) |
| AR (1) | AR003416A1 (fr) |
| AU (1) | AU701187B2 (fr) |
| BG (1) | BG102008A (fr) |
| BR (1) | BR9608063A (fr) |
| CA (1) | CA2218325A1 (fr) |
| CZ (1) | CZ327997A3 (fr) |
| EA (1) | EA000278B1 (fr) |
| HR (1) | HRP960167A2 (fr) |
| HU (1) | HUP9801651A3 (fr) |
| IL (2) | IL117879A0 (fr) |
| MA (1) | MA23843A1 (fr) |
| MX (1) | MX9708016A (fr) |
| PE (1) | PE44097A1 (fr) |
| PL (1) | PL322907A1 (fr) |
| SK (1) | SK140597A3 (fr) |
| TR (1) | TR199701202T1 (fr) |
| WO (1) | WO1996033164A1 (fr) |
| YU (1) | YU24196A (fr) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2754254B1 (fr) * | 1996-10-09 | 1998-10-30 | Rhone Poulenc Agrochimie | Fongicides a groupes hydroximiques et hydrazoniques |
| FR2777002A1 (fr) * | 1998-04-07 | 1999-10-08 | Rhone Poulenc Agrochimie | Nouveaux composes fongicides |
| FR2777003A1 (fr) * | 1998-04-07 | 1999-10-01 | Rhone Poulenc Agrochimie | Nouveaux composes fongicides |
| FR2798929A1 (fr) * | 1999-09-28 | 2001-03-30 | Aventis Cropscience Sa | Nouveaux composes fongicides optiquement actifs |
| FR2799460A1 (fr) * | 1999-10-07 | 2001-04-13 | Aventis Cropscience Sa | Procede de preparation de compose hydroximique |
| US6849996B2 (en) * | 2003-05-30 | 2005-02-01 | General Electric Company | Electrode materials for electric lamps and methods of manufacture thereof |
| JP2007269732A (ja) * | 2006-03-31 | 2007-10-18 | Asahi Kasei Fainkemu Kk | ビスヒドロキサム酸の製造方法 |
| KR101690631B1 (ko) | 2007-11-27 | 2017-01-09 | 알지파마 아이피알 에이에스 | 바이오필름 퇴치에 있어서의 알기네이트 올리고머의 용도 |
| EP2231591B1 (fr) | 2007-12-06 | 2015-02-11 | Kyung Nong Corporation | Composés méthoxyimino et composition fongicide comprenant de tels composés |
| GB201116010D0 (en) * | 2011-09-15 | 2011-10-26 | Algipharma As | Use of alginate oligomers to enhance the effects of antifungal agents |
| WO2017130679A1 (fr) * | 2016-01-29 | 2017-08-03 | 住友化学株式会社 | Procédé de production de composé thiocarbonyle |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2118769T3 (es) * | 1988-11-21 | 1998-10-01 | Zeneca Ltd | Fungicidas. |
| ATE136543T1 (de) * | 1989-01-11 | 1996-04-15 | Agrevo Uk Ltd | Acrylat-fungizide |
| ATE141589T1 (de) * | 1989-05-17 | 1996-09-15 | Shionogi & Co | Alkoxyiminoacetamid-derivate und ihre verwendung als pilztötendes mittel |
| US5104872A (en) * | 1989-08-22 | 1992-04-14 | Nihon Hohyaku Co., Ltd. | N-(substituted benzyloxy) imine derivatives and method of use thereof |
| EP0426460A1 (fr) * | 1989-11-02 | 1991-05-08 | Ube Industries, Ltd. | Dérivés d'éthers d'oxime, leur préparation et germicides les contenant |
| DK0669319T3 (da) * | 1990-06-27 | 1999-02-08 | Basf Ag | O-benzyloximethere og plantebeskyttelsesmidler indeholdende disse forbindelser |
| US5194622A (en) * | 1990-11-21 | 1993-03-16 | Roussel Uclaf | Process for preparation of thiazolylalkoxy acrylates |
| JP2828186B2 (ja) * | 1991-09-13 | 1998-11-25 | 宇部興産株式会社 | アクリレート系化合物、その製法及び殺菌剤 |
| JP3121061B2 (ja) * | 1991-10-04 | 2000-12-25 | 塩野義製薬株式会社 | アルコキシイミノアセトアミド類製造用中間体の製造法およびそれに用いる中間体 |
| EP0585751B1 (fr) * | 1992-08-29 | 1996-10-23 | BASF Aktiengesellschaft | N-Méthylamides, procédé pour leur préparation et intermédiaires et leur utilisation comme pesticides |
| GB9226865D0 (en) * | 1992-12-23 | 1993-02-17 | Ici Plc | Fungicides |
| DE4305502A1 (de) * | 1993-02-23 | 1994-08-25 | Basf Ag | Ortho-substituierte 2-Methoxyiminophenylessigsäuremethylamide |
| DE69406483T2 (de) * | 1993-03-19 | 1998-03-19 | Ube Industries | Oximetherverbindungen, Verfahren zur Herstellung derselben und Fungizide, die sie enthalten |
| JP2004039759A (ja) * | 2002-07-01 | 2004-02-05 | Taga Seisakusho:Kk | コイルボビンの端子と被覆導線の接合方法 |
-
1995
- 1995-07-31 JP JP7194670A patent/JPH093031A/ja active Pending
-
1996
- 1996-01-11 MX MX9708016A patent/MX9708016A/es unknown
- 1996-01-11 BR BR9608063A patent/BR9608063A/pt unknown
- 1996-03-29 KR KR1019970707379A patent/KR19990007856A/ko not_active Withdrawn
- 1996-03-29 WO PCT/EP1996/001386 patent/WO1996033164A1/fr not_active Ceased
- 1996-03-29 AP APAP/P/1997/001140A patent/AP9701140A0/en unknown
- 1996-03-29 PL PL96322907A patent/PL322907A1/xx unknown
- 1996-03-29 AU AU54977/96A patent/AU701187B2/en not_active Ceased
- 1996-03-29 CA CA002218325A patent/CA2218325A1/fr not_active Abandoned
- 1996-03-29 EA EA199700317A patent/EA000278B1/ru not_active IP Right Cessation
- 1996-03-29 HU HU9801651A patent/HUP9801651A3/hu unknown
- 1996-03-29 CZ CZ973279A patent/CZ327997A3/cs unknown
- 1996-03-29 SK SK1405-97A patent/SK140597A3/sk unknown
- 1996-03-29 JP JP08531441A patent/JP2001500470A/ja active Pending
- 1996-03-29 EP EP96911965A patent/EP0821667A1/fr not_active Ceased
- 1996-03-29 US US08/945,343 patent/US5919825A/en not_active Expired - Fee Related
- 1996-03-29 TR TR97/01202T patent/TR199701202T1/xx unknown
- 1996-04-11 IL IL11787996A patent/IL117879A0/xx unknown
- 1996-04-12 PE PE1996000259A patent/PE44097A1/es not_active Application Discontinuation
- 1996-04-12 HR HRPTC/IB96/00276A patent/HRP960167A2/hr not_active Application Discontinuation
- 1996-04-15 AR ARP960102196A patent/AR003416A1/es unknown
- 1996-04-16 MA MA24203A patent/MA23843A1/fr unknown
- 1996-04-17 YU YU24196A patent/YU24196A/sh unknown
-
1997
- 1997-10-30 BG BG102008A patent/BG102008A/xx unknown
-
1998
- 1998-12-30 US US09/222,870 patent/US5990161A/en not_active Expired - Fee Related
-
1999
- 1999-11-07 IL IL13279099A patent/IL132790A0/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0821667A1 (fr) | 1998-02-04 |
| YU24196A (sh) | 1998-11-05 |
| MX9708016A (es) | 1998-06-28 |
| US5919825A (en) | 1999-07-06 |
| JPH093031A (ja) | 1997-01-07 |
| AR003416A1 (es) | 1998-08-05 |
| EA199700317A1 (ru) | 1998-04-30 |
| AP9701140A0 (en) | 1998-01-31 |
| BR9608063A (pt) | 1999-02-17 |
| BG102008A (en) | 1998-09-30 |
| HUP9801651A3 (en) | 1999-01-28 |
| AU701187B2 (en) | 1999-01-21 |
| PE44097A1 (es) | 1997-10-13 |
| EA000278B1 (ru) | 1999-02-25 |
| AU5497796A (en) | 1996-11-07 |
| KR19990007856A (ko) | 1999-01-25 |
| MA23843A1 (fr) | 1996-12-31 |
| PL322907A1 (en) | 1998-03-02 |
| JP2001500470A (ja) | 2001-01-16 |
| IL132790A0 (en) | 2001-03-19 |
| IL117879A0 (en) | 1996-08-04 |
| SK140597A3 (en) | 1998-05-06 |
| WO1996033164A1 (fr) | 1996-10-24 |
| HUP9801651A2 (hu) | 1998-10-28 |
| US5990161A (en) | 1999-11-23 |
| TR199701202T1 (xx) | 1998-03-21 |
| CZ327997A3 (cs) | 1998-02-18 |
| CA2218325A1 (fr) | 1996-10-24 |
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