FI66348C - Som fungicider anvaendbara 3-klor-n-(substituerad-fenyl)-2,6-dinitro-4-(trifluormetyl)bensenamin-derivat - Google Patents
Som fungicider anvaendbara 3-klor-n-(substituerad-fenyl)-2,6-dinitro-4-(trifluormetyl)bensenamin-derivat Download PDFInfo
- Publication number
- FI66348C FI66348C FI790141A FI790141A FI66348C FI 66348 C FI66348 C FI 66348C FI 790141 A FI790141 A FI 790141A FI 790141 A FI790141 A FI 790141A FI 66348 C FI66348 C FI 66348C
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- FI
- Finland
- Prior art keywords
- chloro
- grams
- dinitro
- trifluoromethyl
- prepared
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- 239000004480 active ingredient Substances 0.000 claims description 16
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- MNRTYHQJFMNVIA-UHFFFAOYSA-N 3-chloro-n-(2,6-dichloro-4-nitrophenyl)-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound ClC1=CC([N+](=O)[O-])=CC(Cl)=C1NC1=C([N+]([O-])=O)C=C(C(F)(F)F)C(Cl)=C1[N+]([O-])=O MNRTYHQJFMNVIA-UHFFFAOYSA-N 0.000 description 1
- WZFOFRISHPCLGD-UHFFFAOYSA-N 3-chloro-n-(2,6-dichlorophenyl)-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=C(Cl)C=CC=C1Cl WZFOFRISHPCLGD-UHFFFAOYSA-N 0.000 description 1
- LWJWSJSVFYFNTL-UHFFFAOYSA-N 3-chloro-n-(2-chloro-4-nitrophenyl)-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound ClC1=CC([N+](=O)[O-])=CC=C1NC1=C([N+]([O-])=O)C=C(C(F)(F)F)C(Cl)=C1[N+]([O-])=O LWJWSJSVFYFNTL-UHFFFAOYSA-N 0.000 description 1
- KSYIQXGBFSISQX-UHFFFAOYSA-N 3-chloro-n-(3,4-dibromophenyl)-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=CC=C(Br)C(Br)=C1 KSYIQXGBFSISQX-UHFFFAOYSA-N 0.000 description 1
- JSTXLMNPQSRGOV-UHFFFAOYSA-N 3-chloro-n-(3,5-dichlorophenyl)-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=CC(Cl)=CC(Cl)=C1 JSTXLMNPQSRGOV-UHFFFAOYSA-N 0.000 description 1
- LOASZRBFZUUGJE-UHFFFAOYSA-N 3-chloro-n-[4-chloro-3-(trifluoromethyl)phenyl]-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=CC=C(Cl)C(C(F)(F)F)=C1 LOASZRBFZUUGJE-UHFFFAOYSA-N 0.000 description 1
- IYFXQLURQKCAAL-UHFFFAOYSA-N 4-[3-chloro-2,6-dinitro-4-(trifluoromethyl)anilino]benzonitrile Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=CC=C(C#N)C=C1 IYFXQLURQKCAAL-UHFFFAOYSA-N 0.000 description 1
- YBAZINRZQSAIAY-UHFFFAOYSA-N 4-aminobenzonitrile Chemical compound NC1=CC=C(C#N)C=C1 YBAZINRZQSAIAY-UHFFFAOYSA-N 0.000 description 1
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 description 1
- ODGIMMLDVSWADK-UHFFFAOYSA-N 4-trifluoromethylaniline Chemical compound NC1=CC=C(C(F)(F)F)C=C1 ODGIMMLDVSWADK-UHFFFAOYSA-N 0.000 description 1
- ASPDJZINBYYZRU-UHFFFAOYSA-N 5-amino-2-chlorobenzotrifluoride Chemical compound NC1=CC=C(Cl)C(C(F)(F)F)=C1 ASPDJZINBYYZRU-UHFFFAOYSA-N 0.000 description 1
- 241001465180 Botrytis Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000222199 Colletotrichum Species 0.000 description 1
- 241000222235 Colletotrichum orbiculare Species 0.000 description 1
- 240000008067 Cucumis sativus Species 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 241000371644 Curvularia ravenelii Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Chemical class 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 241001123669 Verticillium albo-atrum Species 0.000 description 1
- 235000009754 Vitis X bourquina Nutrition 0.000 description 1
- 235000012333 Vitis X labruscana Nutrition 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- 235000012255 calcium oxide Nutrition 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- BIXZHMJUSMUDOQ-UHFFFAOYSA-N dichloran Chemical compound NC1=C(Cl)C=C([N+]([O-])=O)C=C1Cl BIXZHMJUSMUDOQ-UHFFFAOYSA-N 0.000 description 1
- 231100000676 disease causative agent Toxicity 0.000 description 1
- 235000021186 dishes Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 238000002513 implantation Methods 0.000 description 1
- 239000003317 industrial substance Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 229910003480 inorganic solid Inorganic materials 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- QYXTUZSLPWKXTJ-UHFFFAOYSA-N n-(2-bromo-4,6-dinitrophenyl)-3-chloro-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC(Br)=C1NC1=C([N+]([O-])=O)C=C(C(F)(F)F)C(Cl)=C1[N+]([O-])=O QYXTUZSLPWKXTJ-UHFFFAOYSA-N 0.000 description 1
- ICTOLDDNQWWSSF-UHFFFAOYSA-N n-(2-bromo-4-methylphenyl)-3-chloro-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound BrC1=CC(C)=CC=C1NC1=C([N+]([O-])=O)C=C(C(F)(F)F)C(Cl)=C1[N+]([O-])=O ICTOLDDNQWWSSF-UHFFFAOYSA-N 0.000 description 1
- ZONOQTUTWQTNMM-UHFFFAOYSA-N n-(2-bromo-4-nitrophenyl)-3-chloro-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound BrC1=CC([N+](=O)[O-])=CC=C1NC1=C([N+]([O-])=O)C=C(C(F)(F)F)C(Cl)=C1[N+]([O-])=O ZONOQTUTWQTNMM-UHFFFAOYSA-N 0.000 description 1
- AYTXQERIVRHVNH-UHFFFAOYSA-N n-[3,5-bis(trifluoromethyl)phenyl]-3-chloro-2,6-dinitro-4-(trifluoromethyl)aniline Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 AYTXQERIVRHVNH-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 235000015927 pasta Nutrition 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000003586 protic polar solvent Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 235000011182 sodium carbonates Nutrition 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 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
- 231100000167 toxic agent Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000002435 venom Substances 0.000 description 1
- 231100000611 venom Toxicity 0.000 description 1
- 210000001048 venom Anatomy 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
- 239000002023 wood Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
-
- 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)
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87319078 | 1978-01-30 | ||
| US05/873,190 US4152460A (en) | 1978-01-30 | 1978-01-30 | 3-Chloro-2,6-dinitro-N-(substituted phenyl)-4-(trifluoromethyl)benzenamines |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI790141A7 FI790141A7 (fi) | 1979-07-31 |
| FI66348B FI66348B (fi) | 1984-06-29 |
| FI66348C true FI66348C (fi) | 1984-10-10 |
Family
ID=25361144
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI790141A FI66348C (fi) | 1978-01-30 | 1979-01-17 | Som fungicider anvaendbara 3-klor-n-(substituerad-fenyl)-2,6-dinitro-4-(trifluormetyl)bensenamin-derivat |
Country Status (33)
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4259347A (en) * | 1978-02-16 | 1981-03-31 | Eli Lilly And Company | Control of phytopathogens using dinitroaniline compounds |
| 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 |
| IL61776A (en) * | 1980-01-08 | 1984-05-31 | Lilly Co Eli | N-(nitrophenyl)-polyfluoroethoxy-benzenamines,their preparation,fungicidal and anticoccidial methods using them |
| 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 |
| EP2826474B1 (en) | 2012-03-14 | 2021-05-26 | Sinochem Corporation | Use of substituted diphenylamine compounds in preparing anti-tumour drugs |
| CN108976167B (zh) * | 2017-06-02 | 2021-12-07 | 沈阳中化农药化工研发有限公司 | 一种取代苯肼类化合物及其应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3764624A (en) * | 1970-08-05 | 1973-10-09 | United States Borax Chem | N-substituted-2,6-dinitro-3-(alkoxy or alkylthio)-4-substituted-aniline compounds |
| US3950377A (en) * | 1972-12-20 | 1976-04-13 | Imperial Chemical Industries Limited | Diphenylamine derivatives |
| GB1405120A (en) * | 1972-12-20 | 1975-09-03 | Ici Ltd | Nitrobenzene derivatives |
-
1978
- 1978-01-30 US US05/873,190 patent/US4152460A/en not_active Expired - Lifetime
-
1979
- 1979-01-17 FI FI790141A patent/FI66348C/fi not_active IP Right Cessation
- 1979-01-17 PT PT7969086A patent/PT69086A/pt unknown
- 1979-01-17 NZ NZ189410A patent/NZ189410A/xx unknown
- 1979-01-17 CA CA000319817A patent/CA1117548A/en not_active Expired
- 1979-01-17 IL IL56443A patent/IL56443A/xx unknown
- 1979-01-17 FR FR7901112A patent/FR2415619A1/fr active Granted
- 1979-01-17 AR AR275200A patent/AR223472A1/es active
- 1979-01-18 BE BE1/9245A patent/BE873550A/xx not_active IP Right Cessation
- 1979-01-18 GT GT197955866A patent/GT197955866A/es unknown
- 1979-01-19 PH PH22087A patent/PH15211A/en unknown
- 1979-01-22 JP JP651879A patent/JPS54109931A/ja active Pending
- 1979-01-23 RO RO7996360A patent/RO76486A/ro unknown
- 1979-01-24 DE DE7979300123T patent/DE2961728D1/de not_active Expired
- 1979-01-24 GB GB7902584A patent/GB2013197B/en not_active Expired
- 1979-01-24 EP EP79300123A patent/EP0003430B1/en not_active Expired
- 1979-01-24 PL PL1979212966A patent/PL117491B1/pl unknown
- 1979-01-24 CH CH72079A patent/CH635568A5/fr not_active IP Right Cessation
- 1979-01-25 BR BR7900462A patent/BR7900462A/pt unknown
- 1979-01-26 ZA ZA79344A patent/ZA79344B/xx unknown
- 1979-01-26 AT AT0060779A patent/AT362962B/de not_active IP Right Cessation
- 1979-01-26 HU HU79EI838A patent/HU181430B/hu unknown
- 1979-01-26 AU AU43727/79A patent/AU525301B2/en not_active Ceased
- 1979-01-26 ES ES477214A patent/ES477214A1/es not_active Expired
- 1979-01-26 LU LU80828A patent/LU80828A1/xx unknown
- 1979-01-27 EG EG56/79A patent/EG13874A/xx active
- 1979-01-29 DK DK36479A patent/DK36479A/da not_active Application Discontinuation
- 1979-01-29 SU SU792714351A patent/SU990080A3/ru active
- 1979-01-29 GR GR58203A patent/GR72749B/el unknown
- 1979-01-29 MX MX797689U patent/MX5371E/es unknown
- 1979-01-30 CS CS79656A patent/CS201022B2/cs unknown
- 1979-01-30 DD DD79210715A patent/DD141772A5/de unknown
- 1979-01-30 IE IE15379A patent/IE47988B1/en unknown
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