CHEBI:39713 - 2-amino-4-methylphenol

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ChEBI Name 2-amino-4-methylphenol
ChEBI ID CHEBI:39713
Definition A hydroxytoluene that is phenol substituted by amino and methyl groups at positions 2 and 4, respectively. It is a metabolite of disperse yellow 3.
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/c1-5-2-3-7(9)6(8)4-5/h2-4,9H,8H2,1H3
InChIKey ZMXYNJXDULEQCK-UHFFFAOYSA-N
SMILES CC1=CC(N)=C(O)C=C1
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): sensitiser
A chemical compound that causes a substantial proportion of exposed people or animals to develop an allergic reaction in normal tissue after repeated exposure to the compound.
xenobiotic metabolite
Any metabolite produced by metabolism of a xenobiotic compound.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-amino-4-methylphenol (CHEBI:39713) has role sensitiser (CHEBI:139492)
2-amino-4-methylphenol (CHEBI:39713) has role xenobiotic metabolite (CHEBI:76206)
2-amino-4-methylphenol (CHEBI:39713) is a hydroxytoluene (CHEBI:24751)
2-amino-4-methylphenol (CHEBI:39713) is a substituted aniline (CHEBI:48975)
IUPAC Name
2-amino-4-methylphenol
Synonyms Sources
(2-hydroxy-5-methylphenyl)amine ChEBI
1-amino-2-hydroxy-5-methylbenzene ChEBI
1-hydroxy-2-amino-4-methylbenzene ChEBI
2-amino-4-cresol ChEBI
2-amino-p-cresol PDBeChem
2-hydroxy-5-methylaniline ChEBI
3-amino-4-hydroxytoluene ChEBI
4-methyl-2-aminophenol ChEBI
4-methyl-o-aminophenol ChEBI
5-methyl-2-hydroxyaniline ChEBI
6-hydroxy-m-toluidine ChEBI
Manual Xrefs Databases
2AC PDBeChem
CPD-7366 MetaCyc
DB04533 DrugBank
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Registry Numbers Types Sources
606494 Reaxys Registry Number Reaxys
95-84-1 CAS Registry Number ChEBI
Citations Waiting for Citations Types Sources
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Last Modified
02 February 2024