Product A71301 is a laboratory grade chemical intended for R&D use only. It can be used for synthesis in a research application.
A71301
2-Aminophenol
99%
Synonym(s):
(2-Hydroxyphenyl)amine, 1-Hydroxy-2-aminobenzene, 2-Amino-1-hydroxybenzene, 2-Aminophenol, 2-Aminophenyl alcohol, 2-Hydroxyaniline, 2-Hydroxybenzenamine, o-Aminohydroxybenzene, o-Hydroxyaniline, o-Hydroxyphenylamine
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5 G
HUF 15,100.00
100 G
HUF 16,900.00
500 G
HUF 48,900.00
About This Item
Linear Formula:
H2NC6H4OH
CAS Number:
Molecular Weight:
109.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-431-1
Beilstein/REAXYS Number:
606075
MDL number:
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Product Name
2-Aminophenol, 99%
InChI key
CDAWCLOXVUBKRW-UHFFFAOYSA-N
InChI
1S/C6H7NO/c7-5-3-1-2-4-6(5)8/h1-4,8H,7H2
SMILES string
Nc1ccccc1O
assay
99%
form
powder
mp
170-175 °C (lit.)
Quality Level
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Related Categories
1 of 4
This Item | 369756 | 162965 | C56352 |
|---|---|---|---|
| assay 99% | assay 99% | assay 99% | assay 99% |
| Quality Level 200 | Quality Level 100 | Quality Level 100 | Quality Level 200 |
| mp 170-175 °C (lit.) | mp 12 °C (lit.) | mp - | mp −25 °C (lit.) |
| form powder | form liquid | form liquid | form liquid |
Application
2-Aminophenol can be used in the synthesis of:
- 2-Oxazolidinone derivatives by reacting with β-aminoalcohols in presence of Pd/C-I2 as a catalyst via oxidative cyclocarbonylation.[1]
- Schiff base transition metal(II) complexes with salicylidene-4-aminoantipyrine.[2]
- 2-Arylbenzoxazoles with aldehydes catalyzed by activated carbon in presence of oxygen atmosphere.[3]
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Muta. 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
334.4 °F - closed cup
flash_point_c
168 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of 2-oxazolidinone catalyzed by palladium on charcoal: a novel and highly effective heterogeneous catalytic system for oxidative cyclocarbonylation of β -aminoalcohols and 2-aminophenol.
Li F and Xia C
J. Catal., 227(2), 542-546 (2004)
Synthesis, spectroscopic characterization, redox, and biological screening studies of some Schiff base transition metal (II) complexes derived from salicylidene-4-aminoantipyrine and 2-aminophenol/2-aminothiophenol.
Raman N, et al.
Synth. React. Inorg. Met.-Org. Chem. , 31(7), 1249-1270 (2001)
Michael M Bittner et al.
Journal of the American Chemical Society, 134(12), 5460-5463 (2012-03-16)
The oxidative ring cleavage of aromatic substrates by nonheme Fe dioxygenases is thought to involve formation of a ferrous-(substrate radical) intermediate. Here we describe the synthesis of the trigonal-bipyramdial complex Fe((Ph2)Tp)(ISQ(tBu)) (2), the first synthetic example of an iron(II) center
Yoshinori Endo et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(43), 13609-13613 (2012-09-13)
Aerobic oxidation: in a biomimetic approach, a mixture of redox catalysts forms couples that effect the aerobic oxidation of a mixture of benzylamine and 2-aminophenol derivatives to give the corresponding benzoxazoles. This biomimetic oxidation proceeds smoothly under mild conditions and
Ericsson D Coy et al.
Organic letters, 12(9), 1976-1979 (2010-03-27)
An efficient and facile synthesis of trans-dihydrobenzofurans has been accomplished from o-aminophenols and phenylpropenes via a novel (one-pot) diastereoselective Pd-catalyzed oxyarylation reaction. The development and optimization of this method is described.
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