CHEBI:55546 - 4-hydroxy-6-methylaniline

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ChEBI Name 4-hydroxy-6-methylaniline ChEBI ID CHEBI:55546 Definition A substituted aniline in which the aniline ring carries 4-hydroxy and 6-methyl 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 C7H9NO Net Charge 0 Average Mass 123.15250 Monoisotopic Mass 123.06841 InChI InChI=1S/C7H9NO/c1-5-4-6(9)2-3-7(5)8/h2-4,9H,8H2,1H3 InChIKey QGNGOGOOPUYKMC-UHFFFAOYSA-N SMILES Cc1cc(O)ccc1N 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-6-methylaniline (CHEBI:55546) has role drug metabolite (CHEBI:49103) 4-hydroxy-6-methylaniline (CHEBI:55546) is a phenols (CHEBI:33853) 4-hydroxy-6-methylaniline (CHEBI:55546) is a substituted aniline (CHEBI:48975) IUPAC Name 4-amino-3-methylphenol INN Source sulfamoxole KEGG DRUG Synonyms Sources 2-Amino-5-hydroxytoluene ChemIDplus 2-Methyl-4-hydroxyaniline NIST Chemistry WebBook 3-Methyl-4-aminophenol NIST Chemistry WebBook 4-Amino-3-methylphenol ChemIDplus 4-Amino-m-cresol ChemIDplus 4-Hydroxy-2-methylaniline NIST Chemistry WebBook 4-hydroxy-6'-methylalanine ChEBI 4-Hydroxy-o-toluidine ChemIDplus 4-OH-6'-methylalanine ChEBI p-Amino-m-cresol NIST Chemistry WebBook p-Hydroxy-o-toluidine NIST Chemistry WebBook Registry Numbers Types Sources 2078803 Beilstein Registry Number Beilstein 2835-99-6 CAS Registry Number ChemIDplus 2835-99-6 CAS Registry Number NIST Chemistry WebBook Citation Type Source 9886437 PubMed citation Europe PMC Last Modified 27 November 2015