CHEBI:55545 - 4-hydroxy-2,6-dimethylaniline

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ChEBI Name 4-hydroxy-2,6-dimethylaniline
ChEBI ID CHEBI:55545
Definition A substituted aniline in which the aniline ring carries 4-hydroxy and 2,6-dimethyl substituents; a urinary metabolite of lidocaine.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C8H11NO
Net Charge 0
Average Mass 137.17900
Monoisotopic Mass 137.08406
InChI InChI=1S/C8H11NO/c1-5-3-7(10)4-6(2)8(5)9/h3-4,10H,9H2,1-2H3
InChIKey GCWYXRHXGLFVFE-UHFFFAOYSA-N
SMILES Cc1cc(O)cc(C)c1N
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): drug metabolite

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ChEBI Ontology
Outgoing 4-hydroxy-2,6-dimethylaniline (CHEBI:55545) has role drug metabolite (CHEBI:49103)
4-hydroxy-2,6-dimethylaniline (CHEBI:55545) is a phenols (CHEBI:33853)
4-hydroxy-2,6-dimethylaniline (CHEBI:55545) is a substituted aniline (CHEBI:48975)
IUPAC Name
4-amino-3,5-dimethylphenol
Synonyms Sources
1,3-Dimethyl-2-amino-5-xylenol ChemIDplus
3,5-Dimethyl-4-aminophenol KEGG COMPOUND
3,5-Dimethyl-4-aminophenol ChemIDplus
4-Amino-3,5-dimethylphenol ChemIDplus
4-Amino-3,5-xylenol ChemIDplus
4-Hydroxy-2,6-dimethylaniline ChemIDplus
Manual Xref Database
C16570 KEGG COMPOUND
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Registry Numbers Types Sources
2082260 Reaxys Registry Number Reaxys
2082260 Beilstein Registry Number Beilstein
3096-70-6 CAS Registry Number KEGG COMPOUND
3096-70-6 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
7955068 PubMed citation Europe PMC
9989796 PubMed citation Europe PMC
Last Modified
27 November 2015