ethiofencarb (CHEBI:38483) (original) (raw)

CHEBI:38483 - ethiofencarb

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
Monoisotopic Mass 225.08235
InChI InChI=1S/C11H15NO2S/c1-3-15-8-9-6-4-5-7-10(9)14-11(13)12-2/h4-7H,3,8H2,1-2H3,(H,12,13)
InChIKey HEZNVIYQEUHLNI-UHFFFAOYSA-N
SMILES CCSCc1ccccc1OC(=O)NC
Roles Classification
Biological Role(s): carbamate insecticide Derivatives of carbamic acid with insecticidal properties of general formula ROC(=O)NR1R2, where ROH is an alcohol, oxime, or phenol and R1 is hydrogen or methyl. Like organophosphate insecticides, they are cholinesterase inhibitors, but carbamate insecticides differ in action from the organophosphates in that the inhibitory effect on cholinesterase is generally brief. EC 3.1.1.7 (acetylcholinesterase) inhibitor An EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that interferes with the action of enzyme acetylcholinesterase (EC 3.1.1.7), which helps breaking down of acetylcholine into choline and acetic acid.
Application(s): carbamate insecticide Derivatives of carbamic acid with insecticidal properties of general formula ROC(=O)NR1R2, where ROH is an alcohol, oxime, or phenol and R1 is hydrogen or methyl. Like organophosphate insecticides, they are cholinesterase inhibitors, but carbamate insecticides differ in action from the organophosphates in that the inhibitory effect on cholinesterase is generally brief. agrochemical An agrochemical is a substance that is used in agriculture or horticulture.

View more via ChEBI Ontology

IUPAC Name
2-[(ethylsulfanyl)methyl]phenyl methylcarbamate
Synonyms Sources
2-((Ethylthio)methyl)phenol methylcarbamate ChemIDplus
2-((Ethylthio)methyl)phenyl methylcarbamate ChemIDplus
alpha-(Ethylthio)-o-tolyl methylcarbamate ChemIDplus
alpha-Ethylthio-o-tolyl methylcarbamate ChemIDplus
Croneton ChemIDplus
Manual Xrefs Databases
275 PPDB
C18649 KEGG COMPOUND
View more database links
Registry Numbers Types Sources
2973224 Beilstein Registry Number Beilstein
29973-13-5 CAS Registry Number KEGG COMPOUND
29973-13-5 CAS Registry Number ChemIDplus
Last Modified
28 July 2014