CHEBI:81731 - tolclofos-methyl

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ChEBI Name tolclofos-methyl
ChEBI ID CHEBI:81731
Definition An organic thiophosphate that is 2,6-dichloro-4-methylphenol in which the hydrogen of the hydroxy group group has been replaced by a dimethoxyphosphorothioyl group. Tolclofos-methyl is a phospholipid biosynthesis inhibitor and fungicide that is used for controlling soil-borne diseases caused by Typhula incarnata, Corticium rolfsii, Typhula ishikariensis, and Rhizoctonia solani.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information ChemicalBook:CB2451996, eMolecules:501452, ZINC000002555394
Download Molfile XML SDF
Formula C9H11Cl2O3PS
Net Charge 0
Average Mass 301.12700
Monoisotopic Mass 299.95436
InChI InChI=1S/C9H11Cl2O3PS/c1-6-4-7(10)9(8(11)5-6)14-15(16,12-2)13-3/h4-5H,1-3H3
InChIKey OBZIQQJJIKNWNO-UHFFFAOYSA-N
SMILES COP(=S)(OC)Oc1c(Cl)cc(C)cc1Cl
Roles Classification
Biological Role(s): antifungal agrochemical
Any substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
Application(s): antifungal agrochemical
Any substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing tolclofos-methyl (CHEBI:81731) has role antifungal agrochemical (CHEBI:86328)
tolclofos-methyl (CHEBI:81731) is a dichlorobenzene (CHEBI:23697)
tolclofos-methyl (CHEBI:81731) is a organic thiophosphate (CHEBI:37512)
IUPAC Name
O-(2,6-dichloro-4-methylphenyl) O,O-dimethyl phosphorothioate
Synonyms Sources
O-(2,6-dichloro-4-methylphenyl)phosphorothioic acid O,O-dimethyl ester ChEBI
O-2,6-dichloro-p-tolyl O,O-dimethyl phosphorothioate Alan Wood's Pesticides
S-3349 ChemIDplus
tolclofos-Me ChEBI
tolclofos-méthyl ChEBI
Brand Names Sources
Basilex NIST Chemistry WebBook
Grancer ChEBI
Risolex NIST Chemistry WebBook
Rizolex ChemIDplus
Manual Xrefs Databases
644 PPDB
C18407 KEGG COMPOUND
DE2501040 Patent
GB1467561 Patent
tolclofos-methyl Alan Wood's Pesticides
View more database links
Registry Numbers Types Sources
2136521 Reaxys Registry Number Reaxys
57018-04-9 CAS Registry Number ChemIDplus
57018-04-9 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations
Last Modified
08 July 2015