tiadinil (CHEBI:81825)

ChEBI > Main

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name	tiadinil

ChEBI ID	CHEBI:81825

Definition	A monocarboxylic acid amide resulting from the formal condensation of the carboxy group of 4-methyl-1,2,3-thiadiazole-5-carboxylic acid with the amino group of 3-chloro-4-methylaniline. It is a fungicide used particularly for the control of fungal diseases in rice.

Stars	This entity has been manually annotated by the ChEBI Team.

Supplier Information

Download	Molfile XML SDF

Formula

C11H10ClN3OS

Net Charge

Average Mass

267.73500

Monoisotopic Mass

267.02331

InChI

InChI=1S/C11H10ClN3OS/c1-6-3-4-8(5-9(6)12)13-11(16)10-7(2)14-15-17-10/h3-5H,1-2H3,(H,13,16)

InChIKey

VJQYLJSMBWXGDV-UHFFFAOYSA-N

SMILES

Cc1nnsc1C(=O)Nc1ccc(C)c(Cl)c1

Roles Classification
Biological Role(s):	antifungal agrochemical Any substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties. fungicide A substance used to destroy fungal pests. (via anilide fungicide ) (via amide fungicide ) antifungal agent An antimicrobial agent that destroys fungi by suppressing their ability to grow or reproduce. (via amide antifungal agent )

Application(s):	antifungal agrochemical Any substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties. fungicide A substance used to destroy fungal pests. (via anilide fungicide ) (via amide fungicide )

ChEBI Ontology
Outgoing	tiadinil (CHEBI:81825) has role antifungal agrochemical (CHEBI:86328) tiadinil (CHEBI:81825) is a anilide fungicide (CHEBI:87015) tiadinil (CHEBI:81825) is a monocarboxylic acid amide (CHEBI:29347) tiadinil (CHEBI:81825) is a monochlorobenzenes (CHEBI:83403) tiadinil (CHEBI:81825) is a organosulfur compound (CHEBI:33261) tiadinil (CHEBI:81825) is a thiadiazoles (CHEBI:38099)

IUPAC Name

N-(3-chloro-4-methylphenyl)-4-methyl-1,2,3-thiadiazole-5-carboxamide

Synonyms	Sources
3'-chloro-4,4'-dimethyl-1,2,3-thiadiazole-5-carboxanilide	Alan Wood's Pesticides
TDL	ChEBI

Last Modified

21 July 2015