A7000
2-Acetamidophenol
97%
Synonym(s):
2′-Hydroxyacetanilide, N-(2-Hydroxyphenyl)acetamide, NSC 3989
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About This Item
Linear Formula:
CH3CONHC6H4OH
CAS Number:
Molecular Weight:
151.16
Beilstein:
607592
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
form
powder
mp
205-210 °C (lit.)
SMILES string
CC(=O)Nc1ccccc1O
InChI
1S/C8H9NO2/c1-6(10)9-7-4-2-3-5-8(7)11/h2-5,11H,1H3,(H,9,10)
InChI key
ADVGKWPZRIDURE-UHFFFAOYSA-N
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Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Huma Jawed et al.
International immunopharmacology, 10(8), 900-905 (2010-05-11)
The present study was carried out to study the anti-arthritic and anti-inflammatory activity of N-(2-hydroxy phenyl) acetamide in adjuvant-induced arthritis in adult female Sprague Dawley rats. During experimental period, body weight and paw oedema volume were observed. At the end
P Anilkumar et al.
Langmuir : the ACS journal of surfaces and colloids, 24(17), 9754-9762 (2008-08-06)
Here, we report a synthesis of novel polyaniline nanospheres bearing mono- and bishydroxyl functional groups to trace the molecular interactions at the nanosurfaces through vitamin C sensing. Two new aniline monomers were synthesized via a tailor-made approach and polymerized to
K Pusecker et al.
The Journal of antibiotics, 50(6), 479-483 (1997-06-01)
The novel 5,10-dihydrophencomycin methyl ester (4) and the known microbial metabolites (2-hydroxyphenyl)-acetamide (1), menaquinone MK9 (II, III, VIII, IX-H8) (2), and phencomycin (3a) were isolated from an unidentified marine Streptomyces sp. and the structures were elucidated by NMR methods. Compound
John P Savaryn et al.
Drug metabolism and disposition: the biological fate of chemicals, 48(7), 594-602 (2020-05-01)
Despite the availability of liquid chromatography (LC)-mass spectrometry (MS) methods for quantifying cytochrome P450 (P450) proteins, incorporation of P450 protein quantification into induction study workflows has not been widely adopted. To more readily enable P450 protein quantification in induction study
M Hamilton et al.
Drug metabolism and disposition: the biological fate of chemicals, 14(1), 5-12 (1986-01-01)
The metabolism of 2- and 3-hydroxyacetanilide was examined in incubations with mouse liver microsomes. Metabolic products were determined by a comparison of both chromatographic and electrochemical properties with that of reference materials. Using this technique, 3-hydroxyacetaminophen and 2-acetamidohydroquinone were positively
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