2-aminophenol

Synonyms: "o-aminophenol", "o-hydroxyaniline", "2-hydroxyaniline", "2-amino-1-hydroxybenzene", "Fouramine OP", "Benzofur GG", "Pelagol Grey GG", "Pelagol 3GA", "Nako Yellow 3GA", "ortho-aminophenol", "BASF ursol 3GA", "Zoba 3GA", "Nako Yellow ga", "2-Hydroxyanaline", "Aminophenol", "o-Hydroxyphenylamine", "Paradone Olive Green B", "Questiomycin B", "2-Aminobenzenol", "1-Hydroxy-2-aminobenzene", "1-Amino-2-hydroxybenzene", "2-amino-phenol".

Source: 2-aminophenol is used as the precursor for indols synthesis.

Identifiers:

IUPAC Name: 2-aminophenol
CAS Number: 95-55-6
PubChem ID: 5801
InChiKey: CDAWCLOXVUBKRW-UHFFFAOYSA-N
Canonical SMILES: C1=CC=C(C(=C1)N)O

Structural Properties:

Molecular Formula: C₆H₇NO
Molecular Weight: 109.128

Pharmacophore Features:

Number of bond donors: 2
Number of bond acceptors: 2
Number of atoms different from hydrogen: 8

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2D structure (.sdf)
3D structure (.sdf)
3D structure (.mol2)
3D structure (.pdb)
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Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors

Rogers, K.S. and Evangelista, S.J., 1985. 3-Hydroxykynurenine, 3-hydroxyanthranilic acid, and o-aminophenol inhibit leucine-stimulated insulin release from rat pancreatic islets. Proceedings of the Society for Experimental Biology and Medicine, 178(2), pp.275-278. DOI: https://doi.org/10.3181/00379727-178-42010. URL: http://journals.sagepub.com/doi/abs/10.3181/00379727-178-42010.