Weight | 109.128 g/mol |
---|---|
Formula | C6H7NO |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2-Aminophenol (27598-85-2, 95-55-6)
2-aminophenol, ion (1+) · 2-aminophenol, monosodium salt · ortho-aminophenol
Score:
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- Amberlite XAD-2 functionalized with o-aminophenol: synthesis and applications as extractant for copper(II), cobalt(II), cadmium(II), nickel(II), zinc(II) and lead(II) (Talanta, 2000)
- Oxidation colorants comprising 2-(2,5-diaminophenyl)-ethanol compounds and 2-chloro-6-methyl-3-aminophenol compounds (1995)
- Spectroscopic study of molecular structures of novel Schiff base derived from o-phthaldehyde and 2-aminophenol and its coordination compounds together with their biological activity. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2009)
- Postnatal development of uridine diphosphate glucuronyltransferase activity towards bilirubin and 2-aminophenol in human liver (Biochemical Journal, 1979)
- 2-aminophenol 1,6-dioxygenase: a novel aromatic ring cleavage enzyme purified from Pseudomonas pseudoalcaligenes JS45. (Journal of Bacteriology, 1996)
- Novel genes encoding 2-aminophenol 1,6-dioxygenase from Pseudomonas species AP-3 growing on 2-aminophenol and catalytic properties of the purified enzyme. (Journal of Biological Chemistry, 1997)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H341: Suspected of causing genetic defects
Warning Germ cell mutagenicity - Category 2 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - 2-aminophenol, ion (1+)
- 2-aminophenol, monosodium salt
- ortho-aminophenol
- 2-aminophenol, monopotassium salt
- 2-aminophenol, hydrochloride
- o-aminophenol
-
SMILESC1=CC=C(C(=C1)N)O
-
InChIKeyCDAWCLOXVUBKRW-UHFFFAOYSA-N
- Pubchem - 2-Aminophenol
- Wikipedia - 2-Aminophenol
2-Aminophenol is an organic compound with the formula | C=6 | H=4 (OH)N| H=2 . Along with its isomer 4-aminophenol, it is an amphoteric molecule and a reducing agent. It is a useful reagent for the synthesis of dyes and heterocyclic compounds.
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