FIELD: chemistry.
SUBSTANCE: invention relates to fungus control, specifically to 5-iodotetrazole derivatives , in which R1 denotes butylene, straight unsubstituted alkyl with 8-16 carbon atoms, straight or branched unsubstituted or mono- or multi-, identically or differently substituted alkyl with 1-8 carbon atoms, where the substitutes are or mono- or multi-, identically or differently substituted alkyl residues selected from a group comprising unsubstituted alkoxy or 1-6 carbon atoms and alkoxy with 1-6 carbon atoms, substituted with dioxalonyl, phenyl which is up to five times identically or differently substituted with halogen, alkyl with 1-4 carbon atoms, halogenalkyl with 1-4 carbon aotms, alkoxy with 1-3 carbon atoms, alkylthio with 1-4 carbon atoms, morpholinyl, except the following compounds: 1-tert-butyl-5-iodotetrazole, 1-ethyl-5-iodotetrazole, 1-methyl-5-iodotetrazole. Said 5-iodotetrazole derivatives are obtained by treating tetrazoles of general formula , in which R1 assumes values given above, with iodine in an organic solvent in the presence of a base and, if needed, in the presence of a diluent. The invention also relates to a fungicidal agent, containing 5-iodotetrazole derivatives of general formula , in which R1 denotes hydrogen, alkylene with 1-4 carbon atoms, straight unsubstituted alkyl with 8-16 carbon atoms, straight or branched unsubstituted or mono- or multi-, identically or differently substituted alkyl with 1-8 carbon atoms, where the substitutes are mono- or multi-, identically or differently substituted alkyl residues selected from a group comprising unsubstituted alkoxy with 1-6 carbon atoms and alkoxy with 1-6 carbon atoms, substituted dioxalonyl, unsubstituted phenyl, phenyl which is up to five times identically or differently substituted with halogen, alkyl with 1-4 carbon atoms, halogenalkyl with 1-4 carbon atoms, alkoxy with 1-3 carbon atoms, alkylthio with 1-4 carbon atoms, morpholinyl and at least one solvent or diluent, as well as auxiliary additives if necessary. The invention also relates to paint material containing compounds of formula (Ia).
EFFECT: said fungicidal agent can be used in a method of protecting plants and paint materials from attack and/or decomposition by fungi by exposing the fungi or habitat thereof to the said agent.
11 cl, 2 tbl
Title | Year | Author | Number |
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1-ALKYL-3,5-DIALYL-1,4-DIHYDROPYRIDINE DERIVATIVES AS MIXTURE OF ISOMERS THEREOF | 1995 |
|
RU2158259C2 |
DERIVATIVES OF CYCLOALKANOINDOLE AND AZAINDOLE, MIXTURE OF THEIR ISOMERS OR SEPARATE ISOMERS AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, DERIVATIVES OF CARBOXYLIC ACID AS PARENT COMPOUNDS AND PHARMACEUTICAL COMPOSITION INHIBITING RELEASE OF LIPOPROTEINS ASSOCIATED WITH APOLIPOPROTEIN B-100 | 1995 |
|
RU2157803C2 |
DERIVATIVES OF 4-ARYL-6-AMINONICOTINIC ACID AND THEIR SALTS | 1995 |
|
RU2154635C2 |
DERIVATIVES OF CYCLOHEXADIENE, MIXTURE OF THEIR ISOMERS OR SEPARATE ISOMERS AND THEIR SALTS AND PHARMACEUTICAL COMPOSITION WITH SELECTIVE MODULATING EFFECT ON CALCIUM-DEPENDENT POTASSIUM CHANNELS OF HIGH CONDUCTIVITY | 1995 |
|
RU2155748C2 |
BENZOTHIOPHEN-2-CARBOXAMINE-5,5-DIOXIDE DERIVATIVES, METHOD OF PREPARATION THEREOF, FUNGICIDAL AND MICROBICIDAL AGENT | 1992 |
|
RU2105763C1 |
DERIVATIVES OF HETEROCYCLE-SUBSTITUTED PHENYLCYCLOHEXANE CARBOXYLIC ACID, MIXTURE OF THEIR ISOMERS OR SEPARATE ISOMERS AND THEIR SALTS | 1994 |
|
RU2125990C1 |
ARYLIDENE-OR ARYLALKYL-1-AZACYCLOALKANE DERIVATIVES, MIXTURES OF ISOMERS THEREOF OF ISOMERS THEREOF OF INDIVIDUAL ISOMERS OR SALTS | 1993 |
|
RU2126400C1 |
CYCLIC NITROGEN-CONTAINING DERIVATIVES, MIXTURE OF THEIR ISOMERS, INDIVIDUAL ISOMERS OR THEIR SALTS | 1994 |
|
RU2126002C1 |
DIHYDROPYRIDINE DERIVATIVES, MIXTURE OF THEIR ISOMERS, INDIVIDUAL ISOMERS OR THEIR PHYSIOLOGICALLY TOLERANTABLE SALTS, METHODS OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS AND METHOD OF THEIR SYNTHESIS | 1992 |
|
RU2081872C1 |
CORROSION-INHIBITION COMPOSITION FOR COATINGS, METHOD OF PREPARATION THEREOF, AND AMINOPHOSPHONIC AND AMINOPHOSPHOROUS ACID DERIVATIVES AND THEIR SALTS | 1997 |
|
RU2164552C2 |
Authors
Dates
2011-05-10—Published
2005-07-19—Filed