RU95118179A - FUNGICIDE MIXTURE - Google Patents
FUNGICIDE MIXTUREInfo
- Publication number
- RU95118179A RU95118179A RU95118179/04A RU95118179A RU95118179A RU 95118179 A RU95118179 A RU 95118179A RU 95118179/04 A RU95118179/04 A RU 95118179/04A RU 95118179 A RU95118179 A RU 95118179A RU 95118179 A RU95118179 A RU 95118179A
- Authority
- RU
- Russia
- Prior art keywords
- triazol
- methyl
- dichlorophenyl
- fluorophenyl
- chlorophenyl
- Prior art date
Links
- 230000000855 fungicidal Effects 0.000 title claims 7
- 239000000417 fungicide Substances 0.000 title claims 3
- 239000000203 mixture Substances 0.000 title claims 3
- 239000000126 substance Substances 0.000 claims 6
- KAESVJOAVNADME-UHFFFAOYSA-N pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims 5
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 claims 4
- STMIIPIFODONDC-UHFFFAOYSA-N Hexaconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 claims 4
- -1 bitirtanol Chemical compound 0.000 claims 4
- 241000233866 Fungi Species 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- DETXAJGVVCIVAK-UHFFFAOYSA-N 1-(2-chlorophenyl)-3,3-dimethyl-2-(1,2,4-triazol-1-ylmethyl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CC1=CC=CC=C1Cl DETXAJGVVCIVAK-UHFFFAOYSA-N 0.000 claims 2
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 claims 2
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims 2
- OVFHHJZHXHZIHT-UHFFFAOYSA-N 3-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)quinazolin-4-one Chemical compound ClC1=CC(Cl)=CC=C1N1C(=O)C2=CC=CC=C2N=C1N1N=CN=C1 OVFHHJZHXHZIHT-UHFFFAOYSA-N 0.000 claims 2
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 claims 2
- PZBPKYOVPCNPJY-UHFFFAOYSA-N Enilconazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 claims 2
- 229960002125 Enilconazole Drugs 0.000 claims 2
- 239000005777 Fenpropidin Substances 0.000 claims 2
- 239000005787 Flutriafol Substances 0.000 claims 2
- 239000005795 Imazalil Substances 0.000 claims 2
- WURBVZBTWMNKQT-UHFFFAOYSA-N Triadimefon Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 claims 2
- 239000005846 Triadimenol Substances 0.000 claims 2
- YTOPFCCWCSOHFV-UHFFFAOYSA-N Tridemorph Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 claims 2
- 239000004480 active ingredient Substances 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- CLIDMUTWHLMPMN-UHFFFAOYSA-N imidazole-1-carboxamide Chemical compound NC(=O)N1C=CN=C1 CLIDMUTWHLMPMN-UHFFFAOYSA-N 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 239000011780 sodium chloride Substances 0.000 claims 2
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 claims 2
- RYAUSSKQMZRMAI-ZACQAIPSSA-N (R)-fenpropimorph Chemical compound C([C@H](C)CC=1C=CC(=CC=1)C(C)(C)C)N1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ZACQAIPSSA-N 0.000 claims 1
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 claims 1
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 claims 1
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims 1
- URDNHJIVMYZFRT-UHFFFAOYSA-N Diclobutrazol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)CC1=CC=C(Cl)C=C1Cl URDNHJIVMYZFRT-UHFFFAOYSA-N 0.000 claims 1
- 239000005760 Difenoconazole Substances 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 239000005778 Fenpropimorph Substances 0.000 claims 1
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N Flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 claims 1
- 239000005813 Penconazole Substances 0.000 claims 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N Phenylacetic acid Natural products OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 claims 1
- 239000005822 Propiconazole Substances 0.000 claims 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N Propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims 1
- 239000005839 Tebuconazole Substances 0.000 claims 1
- PXMNMQRDXWABCY-UHFFFAOYSA-N Tebuconazole Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims 1
- 239000005840 Tetraconazole Substances 0.000 claims 1
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 claims 1
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 229960003424 phenylacetic acid Drugs 0.000 claims 1
- 239000003279 phenylacetic acid Substances 0.000 claims 1
- 239000002689 soil Substances 0.000 claims 1
- 230000002195 synergetic Effects 0.000 claims 1
- DKQYGRHMWRXCNF-UHFFFAOYSA-N Cc(cccc1)c1OC(C1)N1C1=C(C)C=CCC1 Chemical compound Cc(cccc1)c1OC(C1)N1C1=C(C)C=CCC1 DKQYGRHMWRXCNF-UHFFFAOYSA-N 0.000 description 1
Claims (4)
б) 4-(2-метил-3-[4-трет. -бутилфенил] -пропил) -2,6-диметилморфолина (фенпропиморф)
или действующего вещества тридеморф либо действующего вещества фенпропидин и в) азольного действующего вещества, выбранного из следующей группы: N-пропил-N- [2,4,6-трихлорфенокси)этил]имидазол-1-карбоксамид формулы
(Z)-2- (1,2,4-триазол-1-илметил) -2- (4-фторфенил) -3-(2-хлорфенил) -оксиран формулы
1-бутил-1-(2,4-дихлорфенил)-2-(1,2,4-триазол-1-ил)-этанол (общепринятое название гексаконазол), 1- [(2-хлорфенил)метил] -1-(1,1-диметил)-2-(1,2,4- триазол-1-ил)-этанол, 1-(4-фторфенил)-1-(2-фторфенил)-2-(1,2,4-триазол-1- ил)-этанол (общепринятое название флутриафол), (RS)-4-(4-хлорфенил)-2- фенил-2-(1Н-1,2,4-триазол-1-илметил)-бутиронитрил, 1-[(2RS,4RS; 2RS,4SR)- 4-бром-2-(2,4-дихлорфенил)-тетрагидрофурфурил] -1Н-1,2,4-триазол, 3-(2,4- дихлорфенил)-2-(1Н-1,2,4-триазол-1-ил)-квиназолин-4(3Н)-он, (RS)-2,2- диметил-3-(2-хлорбензил)-4-(1Н-1,2,4-триазол-1-ил)-бутан-3-ол, битертанол, триадимефон, триадименол, ципроконазолы, дихлобутразол, дифеноконазолы, диниконазолы, этаконазолы, пропиконазолы, флусилазолы, тебуконазолы, имазалил, пенконазолы, тетраконазолы, или соли одного из таких азольных действующих веществ.1. A fungicidal preparation containing a certain amount of a mixture of fungicidal action from a) α-methoxymino-2 - [(2-methylphenoxy) -methyl] methyl ester) - phenylacetic acid and
b) 4- (2-methyl-3- [4-tert. -butylphenyl] -propyl) -2,6-dimethylmorpholine (fenpropimorph)
or the active substance tridemorph or the active substance fenpropidin and c) an azole active substance selected from the following group: N-propyl-N- [2,4,6-trichlorophenoxy) ethyl] imidazole-1-carboxamide of the formula
(Z) -2- (1,2,4-triazol-1-ylmethyl) -2- (4-fluorophenyl) -3- (2-chlorophenyl) -oxirane of the formula
1-butyl-1- (2,4-dichlorophenyl) -2- (1,2,4-triazol-1-yl) -ethanol (common name hexaconazole), 1- [(2-chlorophenyl) methyl] -1- (1,1-dimethyl) -2- (1,2,4-triazol-1-yl) -ethanol, 1- (4-fluorophenyl) -1- (2-fluorophenyl) -2- (1,2,4 -triazol-1-yl) -ethanol (common name flutriafol), (RS) -4- (4-chlorophenyl) -2-phenyl-2- (1H-1,2,4-triazol-1-ylmethyl) -butyronitrile , 1 - [(2RS, 4RS; 2RS, 4SR) - 4-bromo-2- (2,4-dichlorophenyl) -tetrahydrofurfuryl] -1H-1,2,4-triazole, 3- (2,4-dichlorophenyl) -2- (1H-1,2,4-triazol-1-yl) -quinazolin-4 (3H) -one, (RS) -2,2-dimethyl-3- (2-chlorobenzyl) -4- (1H -1,2,4-triazol-1-yl) butane-3-ol, bitirtanol, triadimefon, triadimenol, cyproconazoles, dichlobut azole, difenoconazole, diniconazole, etakonazoly, propiconazole, flusilazole, tebuconazole, imazalil, penconazole, tetraconazole or a salt of one of these azole active ingredients.
б) 4-(2-метил-3-[4-трет. -бутилфенил] -пропил)-2,6-диметилморфолинафенпропиморф)
или действующего вещества тридеморф либо действующего вещества фенпропидин и в) азольного действующего вещества, выбранного из следующей группы: N-пропил-N- [2,4,6-трихлорфенокси)этил]имидазол-1-карбоксамид формулы
(Z) -2- (1,2,4-триазол-1-илметил) -2- (4-фторфенил) -3-(2-хлорфенил) -оксиран формулы
1-бутил-1-(2,4-дихлорфенил) -2- (1,2,4-триазол-1-ил) -этанол (общепринятое название гексаконазол), 1- [(2-хлорфенил)метил] -1-(1,1-диметил)-2-(1,2,4- риазол-1-ил)-этанол, 1-(4-фторфенил)-1-(2-фторфенил)-2-(1,2,4-триазол-1- ил)-этанол (общепринятое название флутриафол), (RS)-4-(4-хлорфенил)-2- фенил-2-(1Н-1,2,4-триазол-1-илметил)-бутиронитрил, 1- [(2RS, 4RS; 2RS, 4RS- 4-бром-2-(2,4-дихлорфенил)-тетрагидрофурфурил] -1Н-1,2,4-триазол, 3-(2,4- дихлорфенил)-2-(1Н-1,2,4-триазол-1-ил)-квиназолин-4(3Н)-он, (SR)-2,2- диметил-3-(2-хлорбензил)-4-(1Н-1,2,4-триазол-1-ил)-бутан-3-ол, битертанол, триадимефон, триадименол, ципроконазолы, дихлобутразол, дифеноконазолы, диниконазолы, этаконазолы, пропиконазолы, флусилазолы, тебуконазолы, имазалил, пенконазолы, тетраконазолы, или соли одного из таких азольных действующих веществ обрабатывают грибы или подвергаемые угрозе поражения грибами материалы, почву, растения или семена.2. The method of combating harmful fungi, characterized in that a certain amount of a mixture of fungicidal action from a) α - [- methoxymino-2 - [(2-methylphenoxy) methyl] -] - phenylacetic acid methyl ester and
b) 4- (2-methyl-3- [4-tert. -butylphenyl] -propyl) -2,6-dimethylmorpholinephenpropimorph)
or the active substance tridemorph or the active substance fenpropidin and c) an azole active substance selected from the following group: N-propyl-N- [2,4,6-trichlorophenoxy) ethyl] imidazole-1-carboxamide of the formula
(Z) -2- (1,2,4-triazol-1-ylmethyl) -2- (4-fluorophenyl) -3- (2-chlorophenyl) -oxirane of the formula
1-butyl-1- (2,4-dichlorophenyl) -2- (1,2,4-triazol-1-yl) -ethanol (common name hexaconazole), 1- [(2-chlorophenyl) methyl] -1- (1,1-dimethyl) -2- (1,2,4-riazol-1-yl) -ethanol, 1- (4-fluorophenyl) -1- (2-fluorophenyl) -2- (1,2,4 -triazol-1-yl) -ethanol (common name flutriafol), (RS) -4- (4-chlorophenyl) -2-phenyl-2- (1H-1,2,4-triazol-1-ylmethyl) -butyronitrile , 1- [(2RS, 4RS; 2RS, 4RS-4-bromo-2- (2,4-dichlorophenyl) -tetrahydrofurfuryl] -1H-1,2,4-triazole, 3- (2,4-dichlorophenyl) - 2- (1H-1,2,4-triazol-1-yl) -quinazolin-4 (3H) -one, (SR) -2,2-dimethyl-3- (2-chlorobenzyl) -4- (1H- 1,2,4-triazol-1-yl) butan-3-ol, bitertanol, triadimefon, triadimenol, cyproconazoles, dichlobu Trazol, difenoconazoles, diniconazoles, ethaconazoles, propiconazoles, flusilazoles, tebuconazoles, imazalil, penconazoles, tetraconazoles, or salts of one of these azole active ingredients treat fungi or endangered fungus materials, soil, plants or seeds.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP4309272,1 | 1993-03-23 | ||
DE4309272A DE4309272A1 (en) | 1993-03-23 | 1993-03-23 | Fungicidal mixture |
DEP4309272.1 | 1993-03-23 | ||
PCT/EP1994/000741 WO1994021123A1 (en) | 1993-03-23 | 1994-03-10 | Fungicidal mixture |
Publications (2)
Publication Number | Publication Date |
---|---|
RU95118179A true RU95118179A (en) | 1997-09-20 |
RU2129371C1 RU2129371C1 (en) | 1999-04-27 |
Family
ID=6483541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU95118179A RU2129371C1 (en) | 1993-03-23 | 1994-03-10 | Fungicide composition and phytopathogenic fungi-control method |
Country Status (18)
Country | Link |
---|---|
EP (1) | EP0690672B1 (en) |
JP (1) | JP3611572B2 (en) |
KR (1) | KR100316043B1 (en) |
CN (1) | CN1119824A (en) |
AT (1) | ATE144371T1 (en) |
AU (1) | AU676031B2 (en) |
CZ (1) | CZ288340B6 (en) |
DE (2) | DE4309272A1 (en) |
DK (1) | DK0690672T3 (en) |
ES (1) | ES2092903T3 (en) |
GR (1) | GR3021492T3 (en) |
HU (1) | HU216718B (en) |
IL (1) | IL108653A (en) |
NZ (1) | NZ263170A (en) |
PL (1) | PL173281B1 (en) |
RU (1) | RU2129371C1 (en) |
UA (1) | UA29473C2 (en) |
WO (1) | WO1994021123A1 (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH11511145A (en) * | 1995-08-17 | 1999-09-28 | ビーエーエスエフ アクチェンゲゼルシャフト | Fungicide mixture |
DE59603180D1 (en) * | 1995-08-17 | 1999-10-28 | Basf Ag | FUNGICIDAL MIXTURES OF AN OXIMETHER CARBONIC ACID WITH AZOLE DERIVATIVES |
EA001085B1 (en) * | 1995-08-18 | 2000-10-30 | Новартис Аг | Microbicidal compositions |
DE19533796A1 (en) * | 1995-09-13 | 1997-03-20 | Basf Ag | Fungicidal mixtures |
EA001225B1 (en) * | 1996-04-11 | 2000-12-25 | Басф Акциенгезельшафт | Fungicidal mixtures |
CN1292658C (en) * | 1997-06-04 | 2007-01-03 | 巴斯福股份公司 | Fungicidal mixture |
DE10347090A1 (en) * | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistic fungicidal drug combinations |
US9090604B2 (en) | 2006-07-27 | 2015-07-28 | E I Du Pont De Nemours And Company | Fungicidal azocyclic amides |
TW200904330A (en) * | 2007-06-15 | 2009-02-01 | Bayer Cropscience Sa | Pesticidal composition comprising a strigolactone derivative and a fungicide compound |
TWI428091B (en) * | 2007-10-23 | 2014-03-01 | Du Pont | Fungicidal mixtures |
TWI489941B (en) * | 2008-09-19 | 2015-07-01 | Sumitomo Chemical Co | Seed treatment agent and method for protecting plant |
CN102017961B (en) * | 2010-12-18 | 2013-06-05 | 陕西美邦农药有限公司 | Bactericidal composition containing tridemorph |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4124255A1 (en) * | 1991-07-22 | 1993-01-28 | Basf Ag | FUNGICIDAL MIXTURE |
DE4130298A1 (en) * | 1991-09-12 | 1993-03-18 | Basf Ag | FUNGICIDAL MIXTURES |
-
1993
- 1993-03-23 DE DE4309272A patent/DE4309272A1/en not_active Withdrawn
-
1994
- 1994-02-15 IL IL10865394A patent/IL108653A/en not_active IP Right Cessation
- 1994-03-10 EP EP94911144A patent/EP0690672B1/en not_active Expired - Lifetime
- 1994-03-10 AT AT94911144T patent/ATE144371T1/en active
- 1994-03-10 JP JP52060394A patent/JP3611572B2/en not_active Expired - Fee Related
- 1994-03-10 CN CN94191547A patent/CN1119824A/en active Pending
- 1994-03-10 DK DK94911144.7T patent/DK0690672T3/en active
- 1994-03-10 DE DE59400914T patent/DE59400914D1/en not_active Expired - Lifetime
- 1994-03-10 RU RU95118179A patent/RU2129371C1/en active
- 1994-03-10 KR KR1019950704059A patent/KR100316043B1/en active IP Right Grant
- 1994-03-10 UA UA95104563A patent/UA29473C2/en unknown
- 1994-03-10 ES ES94911144T patent/ES2092903T3/en not_active Expired - Lifetime
- 1994-03-10 NZ NZ263170A patent/NZ263170A/en not_active IP Right Cessation
- 1994-03-10 CZ CZ19952456A patent/CZ288340B6/en not_active IP Right Cessation
- 1994-03-10 AU AU63760/94A patent/AU676031B2/en not_active Expired
- 1994-03-10 PL PL94310805A patent/PL173281B1/en unknown
- 1994-03-10 WO PCT/EP1994/000741 patent/WO1994021123A1/en active IP Right Grant
- 1994-03-10 HU HU9502779A patent/HU216718B/en unknown
-
1996
- 1996-10-30 GR GR960402861T patent/GR3021492T3/en unknown
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