CHEBI:82288 - o-anisidine

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ChEBI Name o-anisidine
ChEBI ID CHEBI:82288
ChEBI ASCII Name o-anisidine
Definition A substituted aniline that is aniline in which the hydrogen ortho to the amino group has been replaced by a methoxy group. It is used as a chemical intermediate in the synthesis of azo pigments and dyes.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C7H9NO
Net Charge 0
Average Mass 123.155
Monoisotopic Mass 123.06841
InChI InChI=1S/C7H9NO/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3
InChIKey VMPITZXILSNTON-UHFFFAOYSA-N
SMILES C1=CC=CC(=C1N)OC
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): genotoxin
A role played by a chemical compound to induce direct or indirect DNA damage. Such damage can potentially lead to the formation of a malignant tumour, but DNA damage does not lead inevitably to the creation of cancerous cells.
Application(s): reagent
A substance used in a chemical reaction to detect, measure, examine, or produce other substances.
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ChEBI Ontology
Outgoing o-anisidine (CHEBI:82288) has role genotoxin (CHEBI:50902)
o-anisidine (CHEBI:82288) has role reagent (CHEBI:33893)
o-anisidine (CHEBI:82288) is a monomethoxybenzene (CHEBI:25235)
o-anisidine (CHEBI:82288) is a primary amino compound (CHEBI:50994)
o-anisidine (CHEBI:82288) is a substituted aniline (CHEBI:48975)
Synonyms Sources
1-amino-2-methoxybenzene ChemIDplus
2-aminoanisole ChemIDplus
2-anisidine ChemIDplus
2-methoxy-1-aminobenzene ChemIDplus
2-methoxyaniline UniProt
2-methoxybenzenamine ChemIDplus
o-aminoanisole NIST Chemistry WebBook
o-anisidine KEGG COMPOUND
o-anisylamine NIST Chemistry WebBook
o-methoxyaniline ChemIDplus
o-methoxyphenylamine ChemIDplus
ortho-aminoanisole ChemIDplus
ortho-anisidine ChemIDplus
Manual Xrefs Databases
C19191 KEGG COMPOUND
O-Anisidine Wikipedia
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Registry Numbers Types Sources
386210 Beilstein Registry Number Beilstein
90-04-0 CAS Registry Number ChemIDplus
90-04-0 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
21187827 PubMed citation Europe PMC
22403159 PubMed citation Europe PMC
28089782 PubMed citation Europe PMC
Last Modified
20 February 2019