DE2509416C2 - Dinitrobenzotrifluoride, Verfahren zu deren Herstellung und diese enthaltende pestizide Zusammensetzungen - Google Patents
Dinitrobenzotrifluoride, Verfahren zu deren Herstellung und diese enthaltende pestizide ZusammensetzungenInfo
- Publication number
- DE2509416C2 DE2509416C2 DE2509416A DE2509416A DE2509416C2 DE 2509416 C2 DE2509416 C2 DE 2509416C2 DE 2509416 A DE2509416 A DE 2509416A DE 2509416 A DE2509416 A DE 2509416A DE 2509416 C2 DE2509416 C2 DE 2509416C2
- Authority
- DE
- Germany
- Prior art keywords
- dinitrobenzotrifluoride
- compound
- mixture
- preparation
- compounds
- 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
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- 239000002270 dispersing agent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 230000012447 hatching Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 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
- 230000001418 larval effect Effects 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- NFEIBWMZVIVJLQ-UHFFFAOYSA-N mexiletine hydrochloride Chemical compound [Cl-].CC([NH3+])COC1=C(C)C=CC=C1C NFEIBWMZVIVJLQ-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 230000002013 molluscicidal effect Effects 0.000 description 1
- 235000019508 mustard seed Nutrition 0.000 description 1
- SXBAZAIZZCNHMO-UHFFFAOYSA-N n-(2-bromo-4-nitrophenyl)-2,4-dinitro-6-(trifluoromethyl)aniline Chemical compound BrC1=CC([N+](=O)[O-])=CC=C1NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1C(F)(F)F SXBAZAIZZCNHMO-UHFFFAOYSA-N 0.000 description 1
- WBLSOXJJVJDAJG-UHFFFAOYSA-N n-(2-chloro-4-nitrophenyl)-2,4-dinitro-6-(trifluoromethyl)aniline Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1C(F)(F)F WBLSOXJJVJDAJG-UHFFFAOYSA-N 0.000 description 1
- BPJXGCFAFDUMIT-UHFFFAOYSA-N n-(4-bromo-2-nitrophenyl)-2,4-dinitro-6-(trifluoromethyl)aniline Chemical compound FC(F)(F)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1NC1=CC=C(Br)C=C1[N+]([O-])=O BPJXGCFAFDUMIT-UHFFFAOYSA-N 0.000 description 1
- RWKIJHJOSKEADR-UHFFFAOYSA-N n-(4-chlorophenyl)-2,4-dinitro-6-(trifluoromethyl)aniline Chemical compound FC(F)(F)C1=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C1NC1=CC=C(Cl)C=C1 RWKIJHJOSKEADR-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- GNMXMJLERKORTE-UHFFFAOYSA-N n-phenyl-2-(trifluoromethyl)aniline Chemical class FC(F)(F)C1=CC=CC=C1NC1=CC=CC=C1 GNMXMJLERKORTE-UHFFFAOYSA-N 0.000 description 1
- PCBLLVOSVHORQA-UHFFFAOYSA-N n-phenyl-4-(trifluoromethyl)aniline Chemical class C1=CC(C(F)(F)F)=CC=C1NC1=CC=CC=C1 PCBLLVOSVHORQA-UHFFFAOYSA-N 0.000 description 1
- XQIJIALOJPIKGX-UHFFFAOYSA-N naphthalene 1,2-oxide Chemical compound C1=CC=C2C3OC3C=CC2=C1 XQIJIALOJPIKGX-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000002688 persistence Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 206010037833 rales Diseases 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/04—Nitro compounds
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds
-
- 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
- A01N37/34—Nitriles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Medicinal Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1024174A GB1430046A (en) | 1974-03-07 | 1974-03-07 | Nitrobenzene derivatives |
GB1617174 | 1974-04-11 | ||
GB4797674 | 1974-11-06 |
Publications (2)
Publication Number | Publication Date |
---|---|
DE2509416A1 DE2509416A1 (de) | 1975-09-25 |
DE2509416C2 true DE2509416C2 (de) | 1985-04-11 |
Family
ID=27256486
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2509416A Expired DE2509416C2 (de) | 1974-03-07 | 1975-03-04 | Dinitrobenzotrifluoride, Verfahren zu deren Herstellung und diese enthaltende pestizide Zusammensetzungen |
Country Status (18)
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4316988A (en) * | 1976-07-21 | 1982-02-23 | Eli Lilly And Company | N-Alkyldiphenylamines |
DE2728536A1 (de) * | 1977-06-24 | 1979-01-11 | Bayer Ag | Neue 2-arylamino-3,5-dinitro- benzotrifluoride |
EP0003259B1 (en) * | 1978-01-18 | 1982-03-24 | Imperial Chemical Industries Plc | N-formylanilido aromatic compounds, process for their preparation and process for the preparation of the corresponding n-phenyl aromatic amino compounds |
US4259347A (en) * | 1978-02-16 | 1981-03-31 | Eli Lilly And Company | Control of phytopathogens using dinitroaniline compounds |
DE2815290A1 (de) * | 1978-04-08 | 1979-10-18 | Bayer Ag | Neue diarylamine, verfahren zu ihrer herstellung und ihre verwendung |
US4309425A (en) | 1979-08-24 | 1982-01-05 | E. I. Du Pont De Nemours And Company | Miticidal, insecticidal, ovicidal and fungicidal N-(N',N'-diarylaminothio)sulfonamides |
EP0026743B1 (de) * | 1979-09-28 | 1983-05-25 | Ciba-Geigy Ag | Hochsubstituierte Diphenylamine, deren Herstellung und deren Verwendung |
US4407820A (en) * | 1981-03-19 | 1983-10-04 | Eli Lilly And Company | Diphenylamine compounds |
IL64149A0 (en) * | 1981-03-19 | 1982-01-31 | Lilly Co Eli | N-alkylated diphenylamine derivatives,method of preparing them and an insecticidal,arachnicidal and ectoparasiticidal composition containing them |
US4423065A (en) * | 1982-05-04 | 1983-12-27 | Eli Lilly And Company | Naphthalenamine insecticides |
FR2594437A1 (fr) * | 1986-02-19 | 1987-08-21 | Rhone Poulenc Agrochimie | Nouveaux derives du cyano-2 benzimidazole, leur preparation, les compositions les contenant et leur utilisation comme fongicide |
CN1073550C (zh) * | 1997-12-15 | 2001-10-24 | 中国科学院上海有机化学研究所 | N-(二硝基三氟甲基)-取代的-2-甲基苯胺衍生物、制备方法及用途 |
US7285520B2 (en) * | 2003-12-01 | 2007-10-23 | Kimberly-Clark Worldwide, Inc. | Water disintegratable cleansing wipes |
CN102199095B (zh) | 2010-03-22 | 2014-04-09 | 中国中化股份有限公司 | 一种取代二苯胺类化合物及其制备与应用 |
KR101599300B1 (ko) | 2012-03-14 | 2016-03-03 | 시노켐 코포레이션 | 치환 디페닐아민 화합물 및 항종양제로서의 용도 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA654690A (en) | 1962-12-25 | Farbenfabriken Bayer Aktiengesellschaft | Trifluoromethyl-nitro-diphenyl-amines and processes for their production | |
US2212825A (en) * | 1937-12-31 | 1940-08-27 | Du Pont | Nitro-trifluoromethyl-aryl amines and process for making them |
BE577941A (US20050075337A1-20050407-C00081.png) * | 1958-04-22 | |||
US3227758A (en) * | 1962-07-10 | 1966-01-04 | Velsicol Chemical Corp | Phenalkylamines |
US3562332A (en) * | 1964-01-28 | 1971-02-09 | Us Air Force | Fluoro-alkyl-substituted polynitroamines |
CH480791A (de) * | 1967-01-17 | 1969-11-15 | Ciba Geigy | Schädlingsbekämpfungsmittel |
US3950377A (en) * | 1972-12-20 | 1976-04-13 | Imperial Chemical Industries Limited | Diphenylamine derivatives |
ZA739415B (en) * | 1972-12-20 | 1974-11-27 | Ici Ltd | Nitrobenzene derivatives |
-
1974
- 1974-03-07 GB GB1024174A patent/GB1430046A/en not_active Expired
-
1975
- 1975-02-25 IE IE397/75A patent/IE40692B1/xx unknown
- 1975-03-02 IL IL46736A patent/IL46736A/xx unknown
- 1975-03-04 CA CA221,274A patent/CA1046528A/en not_active Expired
- 1975-03-04 DE DE2509416A patent/DE2509416C2/de not_active Expired
- 1975-03-06 BR BR1332/75A patent/BR7501332A/pt unknown
- 1975-03-06 IT IT21014/75A patent/IT1058298B/it active
- 1975-03-06 FR FR7507003A patent/FR2263226B1/fr not_active Expired
- 1975-03-06 OA OA55434A patent/OA04968A/xx unknown
- 1975-03-07 JP JP50027214A patent/JPS50126826A/ja active Pending
- 1975-03-07 HU HUIE678A patent/HU169714B/hu unknown
- 1975-03-07 CS CS751545A patent/CS191259B2/cs unknown
- 1975-03-07 CH CH292275A patent/CH570108A5/xx not_active IP Right Cessation
- 1975-03-07 AR AR257878A patent/AR216422A1/es active
- 1975-03-07 DK DK094075A patent/DK150901C/da not_active IP Right Cessation
- 1975-03-07 US US05/556,421 patent/US4117167A/en not_active Expired - Lifetime
- 1975-03-07 NL NLAANVRAGE7502725,A patent/NL183216C/xx not_active IP Right Cessation
-
1979
- 1979-02-28 SE SE7901811A patent/SE7901811L/xx not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
IE40692B1 (en) | 1979-08-01 |
US4117167A (en) | 1978-09-26 |
SE7901811L (sv) | 1979-02-28 |
GB1430046A (en) | 1976-03-31 |
CS191259B2 (en) | 1979-06-29 |
OA04968A (fr) | 1980-10-31 |
NL183216B (nl) | 1988-04-05 |
DK150901C (da) | 1987-11-23 |
DE2509416A1 (de) | 1975-09-25 |
DK94075A (US20050075337A1-20050407-C00081.png) | 1975-09-08 |
FR2263226B1 (US20050075337A1-20050407-C00081.png) | 1979-10-19 |
IL46736A (en) | 1979-09-30 |
AR216422A1 (es) | 1979-12-28 |
DK150901B (da) | 1987-07-13 |
CH570108A5 (US20050075337A1-20050407-C00081.png) | 1975-12-15 |
IE40692L (en) | 1975-09-07 |
BR7501332A (pt) | 1975-12-09 |
NL183216C (nl) | 1988-09-01 |
IL46736A0 (en) | 1975-05-22 |
AU7872075A (en) | 1976-09-09 |
FR2263226A1 (US20050075337A1-20050407-C00081.png) | 1975-10-03 |
IT1058298B (it) | 1982-04-10 |
CA1046528A (en) | 1979-01-16 |
JPS50126826A (US20050075337A1-20050407-C00081.png) | 1975-10-06 |
NL7502725A (nl) | 1975-09-09 |
HU169714B (US20050075337A1-20050407-C00081.png) | 1977-02-28 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8110 | Request for examination paragraph 44 | ||
D2 | Grant after examination | ||
8364 | No opposition during term of opposition |