CHEBI:189411 - 4'-(4-fluorophenyl)acetanilide

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ChEBI Name 4'-(4-fluorophenyl)acetanilide
ChEBI ID CHEBI:189411
Definition A biphenyl that is 1,1'-biphenyl substituted by a fluoro group at position 4 and a acetylamino group at position 4'. It induces neoplastic lesions in rats.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C14H12FNO
Net Charge 0
Average Mass 229.254
Monoisotopic Mass 229.09029
InChI InChI=1S/C14H12FNO/c1-10(17)16-14-8-4-12(5-9-14)11-2-6-13(15)7-3-11/h2-9H,1H3,(H,16,17)
InChIKey JORMZLCKCZMVJM-UHFFFAOYSA-N
SMILES CC(=O)NC1=CC=C(C=C1)C1=CC=C(F)C=C1
Roles Classification
Biological Role(s): carcinogenic agent
A role played by a chemical compound which is known to induce a process of carcinogenesis by corrupting normal cellular pathways, leading to the acquistion of tumoral capabilities.
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ChEBI Ontology
Outgoing 4'-(4-fluorophenyl)acetanilide (CHEBI:189411) has role carcinogenic agent (CHEBI:50903)
4'-(4-fluorophenyl)acetanilide (CHEBI:189411) is a N-acetylarylamine (CHEBI:13790)
4'-(4-fluorophenyl)acetanilide (CHEBI:189411) is a biphenyls (CHEBI:22888)
4'-(4-fluorophenyl)acetanilide (CHEBI:189411) is a monofluorobenzenes (CHEBI:83575)
4'-(4-fluorophenyl)acetanilide (CHEBI:189411) is a secondary carboxamide (CHEBI:140325)
IUPAC Name
N-(4'-fluoro[biphenyl]-4-yl)acetamide
Synonyms Sources
4'-(4-fluorophenyl)acetanilide ChEBI
4'-(p-fluorophenyl)acetanilide ChemIDplus
4'-fluoro-4-acetylaminobiphenyl ChemIDplus
4'-fluoro-4-biphenylacetamide ChemIDplus
4-acetylamino-4'-fluorobiphenyl ChEBI
FBPA
Note: (2022-01-20) Used as an abbreviation.
 ChEBI
N-(4'-fluoro(1,1'-biphenyl)-4-yl)acetamide ChemIDplus
N-(4'-fluoro-4-biphenyl)acetamide ChEBI
N-(4'-fluoro-4-biphenylyl)acetamide ChemIDplus
N-(4'-fluoro[1,1'-biphenyl]-4-yl)acetamide IUPAC
N-4-(4'-fluoro)biphenylacetamide ChemIDplus
N-4-(4'-fluorobiphenyl)acetamide ChEBI
N-[4-(4-fluorophenyl)phenyl]acetamide ChEBI
N-{4'-fluoro-[1,1'-biphenyl]-4-yl}acetamide ChEBI
Manual Xref Database
9429 ChemSpider
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Registry Numbers Types Sources
2806508 Reaxys Registry Number Reaxys
398-32-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
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Last Modified
20 January 2022