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Merck
모든 사진(3)

주요 문서

H18607

Sigma-Aldrich

2′-Hydroxyacetophenone

ReagentPlus®, 99%

동의어(들):

2-Acetylphenol

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About This Item

Linear Formula:
HOC6H4COCH3
CAS Number:
Molecular Weight:
136.15
Beilstein:
386123
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

4.7 (vs air)

Quality Level

vapor pressure

~0.2 mmHg ( 20 °C)

제품 라인

ReagentPlus®

분석

99%

형태

liquid

refractive index

n20/D 1.558 (lit.)

bp

213 °C/717 mmHg (lit.)

mp

3-6 °C (lit.)

density

1.133 g/mL at 20 °C
1.131 g/mL at 25 °C (lit.)

SMILES string

CC(=O)c1ccccc1O

InChI

1S/C8H8O2/c1-6(9)7-4-2-3-5-8(7)10/h2-5,10H,1H3

InChI key

JECYUBVRTQDVAT-UHFFFAOYSA-N

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법적 정보

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point (°F)

222.8 °F - closed cup

Flash Point (°C)

106 °C - closed cup

개인 보호 장비

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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문서 라이브러리 방문

Daniele Gabriel et al.
Journal of cardiovascular pharmacology, 57(1), 20-27 (2011-01-15)
Isatin (1H-indole-2,3 dione) is an endogenous compound with biological activities. Many of its derivatives have pharmacological effects, including inhibition of cyclic guanosine monophosphate levels in cardiac tissue; sedative-hypnotic profiles; anticonvulsant, analgesic, antithermic, and anti-inflammatory activities; and anxiolytic, antimicrobial, and proapoptotic
Xiao-Feng Wu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(40), 12595-12598 (2012-08-29)
Flavone of the month: a general and efficient method for the palladium-catalyzed carbonylative synthesis of flavones has been developed. Starting from aryl bromides and 2-hydroxyacetophenones, the corresponding flavones have been isolated in good yields.
R R Zaky et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 81(1), 28-34 (2011-07-26)
Schiff base complexes of Cu(II), Ni(II) and Zn(II) with the o-hydroxyacetophenone [N-(3-hydroxy-2-naphthoyl)] hydrazone (H(2)o-HAHNH) containing N and O donor sites have been synthesized. Both ligand and its metal complexes were characterized by different physicochemical methods, elemental analysis, molar conductivity ((1)H
R R Zaky et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 97, 683-694 (2012-08-14)
The o-Hydroxy acetophenone [N-(3-hydroxy-2-naphthoyl)] hydrazone (H(2)o-HAHNH) has been prepared and its structure is confirmed by elemental analysis, IR, (1)H NMR and (13)C NMR spectroscopy. It has been used to produce diverse complexes with Co(II), Cd(II), Hg(II) and U(VI)O(2) ions. The
Shuai Chen et al.
Organic letters, 14(11), 2806-2809 (2012-05-17)
Flavin catalysts perform the first organocatalytic Dakin oxidation of electron-rich arylaldehydes to phenols under mild, basic conditions. Catechols are readily prepared, and the oxidation of 2-hydroxyacetophenone was achieved. Aerobic oxidation is displayed in the presence of Zn(0) as a reducing

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