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US 12,745,775 B2Granted
Agrochemical composition comprising 3-substituted phenylamidine compounds and use thereof
AssigneePi Industries Ltd.
InventorsVishal A. Mahajan, Santosh Shridhar Autkar, Siddaramaiah C R, Hagalavadi M Venkatesha
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Abstract
The present invention discloses a novel agrochemical composition comprising (1) at least one compound of formula (I) wherein, R1, R2, R3, R4, R5, R6, R7 and n are as defined in the detailed description and (2) at least one further active ingredient. The present invention further discloses a method for controlling the phytopathogenic fungi of plants using the agrochemical composition according to invention.
Claims10
A synergistic agrochemical composition comprising a mixture of component (1) and component (2),
- wherein the component (1) is selected from:
- (I-1) N′-(5-chloro-2-methyl-3-(3-methylbenzyl) phenyl)-N-ethyl-N-methylformimidamide;
- (I-2) N′-(2,5-dimethyl-3-(4-methylbenzyl) phenyl)-N-ethyl-N-methylformimidamide;
- (I-3) N′-(2,5-dimethyl-3-(2-methylbenzyl) phenyl)-N-ethyl-N-methylformimidamide;
- (I-4) N-ethyl-N′-(3-(3-fluorobenzyl)-2,5-dimethylphenyl)-N-methylformimidamide;
- (I-5) N-ethyl-N′-(5-fluoro-2-methyl-3-(3-methylbenzyl) phenyl)-N-methylformimidamide;
- or salts, N-oxides, or stereoisomers thereof;
- and the component (2) is selected from the group consisting of:
- (A) inhibitors of the sterol synthesis,
- (B) inhibitors of the respiratory chain at complex I or II,
- (C) inhibitors of the respiratory chain at complex III,
- (E) compounds capable of having a multisite action,
- (K) inhibitors of the melanine biosynthesis,
- (N) compounds capable of acting as uncoupler,
- (O) other fungicides, and
- (P) inhibitors of histone deacetylase,
- wherein
- (A) Inhibitors of the sterol biosynthesis are selected from (A002) difenoconazole, (A003) epoxiconazole, (A006) fenpropimorph, (A009) flutriafol, (A018) prothioconazole, (A021) tebuconazole, (A081) mefentrifluconazole, and (A091) triforine;
- (B) Inhibitors of the respiratory chain at complex I or II are selected from (B001) benzovindiflupyr, (B002) bixafen, (B003) boscalid, (B005) fluopyram, (B007) fluxapyroxad, (B019) pydiflumetofen, (B028) 3-(difluoromethyl)-1-methyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydro-IH-inden-4-yl]-IH-pyrazole-4-carboxamide (inpyrfluxam), (B030) 3-(difluoromethyl)-N-(7-fluoro-1,1,3-trimethyl-2,3-dihydro-IH-inden-4-yl)-1-methyl-1H-pyrazole-4-carboxamide (Fluindapyr), (B038) N-(5-chloro-2-isopropylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-IH-pyrazole-4-carboxamide (isoflucpyram), (B065) thifluzamide, and (B069) cyclobutrifluram;
- (C) Inhibitors of the respiratory chain at complex III are selected from (C003) azoxystrobin, (C014) metominostrobin, (C016) picoxystrobin, (C017) pyraclostrobin, (C020) trifloxystrobin, (C030) 1-(2-{[1-(4-chlorophenyl) pyrazol-3-yl]oxymethyl}-3-methylphenyl)-1,4-dihydro-4-methyl-5H-tetrazol-5-one (Metyltetraprole), (C031) florylpicoxamid, and (C034) metarylpicoxamid;
- (E) Compounds capable to have a multisite action are selected from (E004) chlorothalonil, (E008) copper oxychloride, (E010) dithianon, (E012) folpet, (E013) mancozeb, (E015) metiram, and (E018) propineb;
- (K) the inhibitor of the melanin biosynthesis is selected from (K001) tricyclazole;
- (N) the compound capable to act as an uncoupler is selected from (N001) fluazinam;
- (O) the other fungicide is selected from (O062) 5-fluoro-4-imino-3-methyl-1-[(4-methylphenyl) sulfonyl]-3,4-dihydropyrimidin-2 (1H)-one;
- and
- (P) the inhibitor of histone deacetylase is selected from (P094) N-(2-fluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide.
23 more elements
Dependencies are inferred from the claim text.