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 Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search 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 View more via ChEBI Ontology 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 View more database links Registry Numbers Types Sources 2082260 Reaxys Registry Number Reaxys 3096-70-6 CAS Registry Number KEGG COMPOUND 3096-70-6 CAS Registry Number ChemIDplus Citations Types Sources 7955068 PubMed citation Europe PMC 9989796 PubMed citation Europe PMC Last Modified 27 November 2015