CHEBI:81734 - phenmedipham

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ChEBI Name phenmedipham
ChEBI ID CHEBI:81734
Definition A carbamate ester that is (3-methylphenyl)carbamic acid in which the hydrogen of the hydroxy group has been replaced by a 3-[(methoxycarbonyl)amino]phenyl group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C16H16N2O4
Net Charge 0
Average Mass 300.30920
Monoisotopic Mass 300.111
InChI InChI=1S/C16H16N2O4/c1-11-5-3-6-12(9-11)18-16(20)22-14-8-4-7-13(10-14)17-15(19)21-2/h3-10H,1-2H3,(H,17,19)(H,18,20)
InChIKey IDOWTHOLJBTAFI-UHFFFAOYSA-N
SMILES COC(=O)Nc1cccc(OC(=O)Nc2cccc(C)c2)c1
Roles Classification
Chemical Role(s): environmental contaminant
Any minor or unwanted substance introduced into the environment that can have undesired effects.
Biological Role(s): xenobiotic
A xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
Application(s): herbicide
A substance used to destroy plant pests.
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ChEBI Ontology
Outgoing phenmedipham (CHEBI:81734) has role environmental contaminant (CHEBI:78298)
phenmedipham (CHEBI:81734) has role herbicide (CHEBI:24527)
phenmedipham (CHEBI:81734) has role xenobiotic (CHEBI:35703)
phenmedipham (CHEBI:81734) is a carbamate ester (CHEBI:23003)
Synonyms Sources
3-(methoxyformamido)phenyl (3-methylphenyl)carbamate Alan Wood's Pesticides
3-[(methoxycarbonyl)amino]phenyl (3-methylphenyl)carbamate ChEBI
3-methoxycarbonyl-N-(3'-methylphenyl)-carbamate ChemIDplus
methyl 3-(3-methylcarbaniloyloxy)carbanilate Alan Wood's Pesticides
Manual Xrefs Databases
516 PPDB
C18420 KEGG COMPOUND
phenmedipham Alan Wood's Pesticides
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Registry Numbers Types Sources
13684-63-4 CAS Registry Number ChemIDplus
2395027 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11409536 PubMed citation Europe PMC
2606004 PubMed citation Europe PMC
7919217 PubMed citation Europe PMC
Last Modified
14 November 2014