CHEBI:81824 - diflufenican

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name diflufenican
Definition A pyridinecarboxamide that is pyridine-3-carboxamide substituted by a 2,4-difluorophenyl group at the carbamoyl nitrogen and a 3-(trifluoromethyl)phenoxy group at position 2.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter jewie
Secondary ChEBI IDs CHEBI:83567
Supplier Information
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Formula C19H11F5N2O2
Net Charge 0
Average Mass 394.29490
Monoisotopic Mass 394.07407
InChI InChI=1S/C19H11F5N2O2/c20-12-6-7-16(15(21)10-12)26-17(27)14-5-2-8-25-18(14)28-13-4-1-3-11(9-13)19(22,23)24/h1-10H,(H,26,27)
SMILES Fc1ccc(NC(=O)c2cccnc2Oc2cccc(c2)C(F)(F)F)c(F)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.
carotenoid biosynthesis inhibitor
Any pathway inhibitor that acts on the carotenoid biosynthesis pathway.
Application(s): herbicide
A substance used to destroy plant pests.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing diflufenican (CHEBI:81824) has role carotenoid biosynthesis inhibitor (CHEBI:138208)
diflufenican (CHEBI:81824) has role environmental contaminant (CHEBI:78298)
diflufenican (CHEBI:81824) has role herbicide (CHEBI:24527)
diflufenican (CHEBI:81824) has role xenobiotic (CHEBI:35703)
diflufenican (CHEBI:81824) is a (trifluoromethyl)benzenes (CHEBI:83565)
diflufenican (CHEBI:81824) is a aromatic ether (CHEBI:35618)
diflufenican (CHEBI:81824) is a pyridinecarboxamide (CHEBI:25529)
Synonym Source
2',4'-Difluoro-2-(alpha,alpha,alpha-trifluoro-m-tolyloxy)nicotinanilide ChemIDplus
Manual Xrefs Databases
235 PPDB
diflufenican Alan Wood's Pesticides
View more database links
Registry Numbers Types Sources
4212494 Reaxys Registry Number Reaxys
83164-33-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
22961490 PubMed citation Europe PMC
23887887 PubMed citation Europe PMC
25096492 PubMed citation Europe PMC
Last Modified
16 August 2017