PH26301A - N-phenylalkylbenzamide fungicides - Google Patents
N-phenylalkylbenzamide fungicides Download PDFInfo
- Publication number
- PH26301A PH26301A PH37724A PH37724A PH26301A PH 26301 A PH26301 A PH 26301A PH 37724 A PH37724 A PH 37724A PH 37724 A PH37724 A PH 37724A PH 26301 A PH26301 A PH 26301A
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- Philippines
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- 238000000034 method Methods 0.000 claims description 31
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- CRPOUZQWHJYTMS-UHFFFAOYSA-N dialuminum;magnesium;disilicate Chemical compound [Mg+2].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] CRPOUZQWHJYTMS-UHFFFAOYSA-N 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- OYFJQPXVCSSHAI-QFPUQLAESA-N enalapril maleate Chemical compound OC(=O)\C=C/C(O)=O.C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CCC1)C(O)=O)CC1=CC=CC=C1 OYFJQPXVCSSHAI-QFPUQLAESA-N 0.000 description 1
- 229940117927 ethylene oxide Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000001207 fluorophenyl group Chemical group 0.000 description 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 description 1
- 239000003517 fume Substances 0.000 description 1
- 244000053095 fungal pathogen Species 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 208000037824 growth disorder Diseases 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 208000006278 hypochromic anemia Diseases 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- 235000011475 lollipops Nutrition 0.000 description 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
- 229920000940 maneb Polymers 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 230000036651 mood Effects 0.000 description 1
- NWJUMMHVDMNYMJ-UHFFFAOYSA-N n-benzyl-1,1,1-trifluoromethanamine Chemical compound FC(F)(F)NCC1=CC=CC=C1 NWJUMMHVDMNYMJ-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 230000017074 necrotic cell death Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- 150000004885 piperazines Chemical class 0.000 description 1
- 244000000003 plant pathogen Species 0.000 description 1
- 238000012809 post-inoculation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001681 protective effect Effects 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
- 150000003230 pyrimidines Chemical class 0.000 description 1
- UKHVLWKBNNSRRR-TYYBGVCCSA-M quaternium-15 Chemical compound [Cl-].C1N(C2)CN3CN2C[N+]1(C/C=C/Cl)C3 UKHVLWKBNNSRRR-TYYBGVCCSA-M 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 238000013207 serial dilution Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/66—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
-
- 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
- A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
-
- 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
- C07C259/12—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 with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines
- C07C259/18—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 with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines having carbon atoms of hydroxamidine groups bound to carbon atoms of six-membered aromatic rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11265787A | 1987-10-26 | 1987-10-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
PH26301A true PH26301A (en) | 1992-04-29 |
Family
ID=22345154
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PH37724A PH26301A (en) | 1987-10-26 | 1988-10-26 | N-phenylalkylbenzamide fungicides |
Country Status (18)
Country | Link |
---|---|
EP (1) | EP0314422B1 (ja) |
JP (1) | JPH01151546A (ja) |
KR (1) | KR890006573A (ja) |
CN (1) | CN1033797A (ja) |
AT (1) | ATE92040T1 (ja) |
AU (1) | AU618560B2 (ja) |
BR (1) | BR8805502A (ja) |
CA (1) | CA1301188C (ja) |
DE (1) | DE3882646T2 (ja) |
DK (1) | DK592688A (ja) |
ES (1) | ES2058308T3 (ja) |
HU (1) | HUT49847A (ja) |
IL (1) | IL88133A0 (ja) |
NZ (1) | NZ226693A (ja) |
PH (1) | PH26301A (ja) |
PT (1) | PT88846B (ja) |
SU (1) | SU1760983A3 (ja) |
ZA (1) | ZA887978B (ja) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW575562B (en) * | 1998-02-19 | 2004-02-11 | Agrevo Uk Ltd | Fungicides |
DE19931116A1 (de) * | 1999-07-06 | 2001-01-11 | Bayer Ag | Verfahren zur Herstellung von Phenethylaminen und neue chemische Verbindungen |
TW200306155A (en) * | 2002-03-19 | 2003-11-16 | Du Pont | Benzamides and advantageous compositions thereof for use as fungicides |
WO2006117356A1 (en) * | 2005-05-03 | 2006-11-09 | Bayer Cropscience Sa | New heterocyclylethylbenzamide derivatives |
TWI435863B (zh) | 2006-03-20 | 2014-05-01 | Nihon Nohyaku Co Ltd | N-2-(雜)芳基乙基甲醯胺衍生物及含該衍生物之蟲害防治劑 |
JP5339055B2 (ja) * | 2006-06-13 | 2013-11-13 | 日産化学工業株式会社 | 水性懸濁状農薬組成物 |
WO2008101975A2 (en) * | 2007-02-22 | 2008-08-28 | Bayer Cropscience Sa | New n-(3-phenylpropyl)benzamide derivatives |
AU2009263249B2 (en) | 2008-06-26 | 2015-03-19 | Nobelpharma Co., Ltd. | Agent for regenerating tympanic membrane or external auditory canal |
UA114287C2 (uk) | 2011-03-02 | 2017-05-25 | Дзе Юніверсіті Оф Токіо | Засіб для боротьби з ендопаразитами |
DK2891492T3 (da) | 2012-08-30 | 2022-11-21 | Univ Tokyo | Endoparasit kontrol middel |
JP6251173B2 (ja) | 2012-08-30 | 2017-12-20 | 国立大学法人 東京大学 | 内部寄生虫防除剤及びその使用方法 |
CN102827022A (zh) * | 2012-09-21 | 2012-12-19 | 西华大学 | 2-乙酰氧基-n-(4-甲氧基苯基)苯甲酰胺及其制备方法和用途 |
US9670162B2 (en) | 2013-03-14 | 2017-06-06 | The Board Of Trustees Of The Leland Stanford Junio | Mitochondrial aldehyde dehyrogenase-2 modulators and methods of use thereof |
BR112016017613A2 (pt) | 2014-03-05 | 2020-11-03 | The University Of Tokyo | Agente e método de controle de endoparasita, derivado de carboxamida e seu uso |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1581075A (ja) * | 1968-07-15 | 1969-09-12 | ||
MC1329A1 (fr) * | 1979-05-17 | 1981-04-21 | Wellcome Found | Aryloxy-et arylamino-alcane-thiocarboxamides,leur preparation et leur application en tant que matieres actives de produits pesticides |
JPS5758657A (en) * | 1980-09-26 | 1982-04-08 | Showa Denko Kk | N-alpha,alpha-dimethylbenzylamide derivative and herbicide |
US4835181A (en) * | 1987-02-18 | 1989-05-30 | Eli Lilly And Company | Anticonvulsant agents using cyano dimethylphenyl benzamides |
EP0324521A3 (en) * | 1988-01-11 | 1991-11-27 | Duphar International Research B.V | Method of treating haematologic diseases and pharmaceutical compositions to be used therefor |
-
1988
- 1988-10-24 KR KR1019880013849A patent/KR890006573A/ko not_active Application Discontinuation
- 1988-10-24 IL IL88133A patent/IL88133A0/xx unknown
- 1988-10-25 EP EP88309998A patent/EP0314422B1/en not_active Expired - Lifetime
- 1988-10-25 HU HU885583A patent/HUT49847A/hu unknown
- 1988-10-25 PT PT88846A patent/PT88846B/pt not_active IP Right Cessation
- 1988-10-25 ZA ZA887978A patent/ZA887978B/xx unknown
- 1988-10-25 CA CA000581224A patent/CA1301188C/en not_active Expired - Lifetime
- 1988-10-25 SU SU884356787A patent/SU1760983A3/ru active
- 1988-10-25 ES ES88309998T patent/ES2058308T3/es not_active Expired - Lifetime
- 1988-10-25 DK DK592688A patent/DK592688A/da not_active Application Discontinuation
- 1988-10-25 NZ NZ226693A patent/NZ226693A/en unknown
- 1988-10-25 DE DE88309998T patent/DE3882646T2/de not_active Expired - Fee Related
- 1988-10-25 AU AU24314/88A patent/AU618560B2/en not_active Ceased
- 1988-10-25 BR BR8805502A patent/BR8805502A/pt not_active Application Discontinuation
- 1988-10-25 AT AT88309998T patent/ATE92040T1/de not_active IP Right Cessation
- 1988-10-26 JP JP63270615A patent/JPH01151546A/ja active Pending
- 1988-10-26 PH PH37724A patent/PH26301A/en unknown
- 1988-10-26 CN CN88107356A patent/CN1033797A/zh active Pending
Also Published As
Publication number | Publication date |
---|---|
PT88846B (pt) | 1993-01-29 |
EP0314422B1 (en) | 1993-07-28 |
ATE92040T1 (de) | 1993-08-15 |
CN1033797A (zh) | 1989-07-12 |
DK592688D0 (da) | 1988-10-25 |
EP0314422A3 (en) | 1991-02-06 |
BR8805502A (pt) | 1989-07-04 |
EP0314422A2 (en) | 1989-05-03 |
DE3882646D1 (de) | 1993-09-02 |
AU618560B2 (en) | 1992-01-02 |
ZA887978B (en) | 1989-08-30 |
NZ226693A (en) | 1990-12-21 |
IL88133A0 (en) | 1989-06-30 |
JPH01151546A (ja) | 1989-06-14 |
CA1301188C (en) | 1992-05-19 |
ES2058308T3 (es) | 1994-11-01 |
AU2431488A (en) | 1989-04-27 |
KR890006573A (ko) | 1989-06-14 |
HUT49847A (en) | 1989-11-28 |
SU1760983A3 (ru) | 1992-09-07 |
DK592688A (da) | 1989-04-27 |
DE3882646T2 (de) | 1994-04-28 |
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