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Merck
모든 사진(2)

Key Documents

445134

Sigma-Aldrich

2-Hydroxyacetophenone

98%

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About This Item

Linear Formula:
C6H5COCH2OH
CAS Number:
Molecular Weight:
136.15
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

98%

mp

86-89 °C (lit.)

SMILES string

OCC(=O)c1ccccc1

InChI

1S/C8H8O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,9H,6H2

InChI key

ZWVHTXAYIKBMEE-UHFFFAOYSA-N

애플리케이션

2-Hydroxyacetophenone can be used as a starting material for the synthesis of:
  • Enantioselective 1R-phenyl-1,2-ethanediol in the presence of a rhodium(III) catalyst by asymmetric transfer hydrogenation.
  • Copper(II) complexes of 2-hydroxyacetophenone N-substituted thiosemicarbazones.
  • Chromium, molybdenum, and ruthenium complexes of 2-hydroxyacetophenone Schiff bases.
  • 2-Hydroxyacetophenone-aroyl hydrazone derivatives for inhibition of copper corrosion in nitric acid.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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문서 라이브러리 방문

Chromium, molybdenum and ruthenium complexes of 2-hydroxyacetophenone Schiff bases
Ali SA, et al.
Journal of Coordination Chemistry, 55(10), 1161-1170 (2002)
Ying-Heng Chen et al.
Journal of agricultural and food chemistry, 65(19), 3965-3974 (2017-04-30)
4-[2-(t-Butylamino)-1-hydroxyethyl]phenol (buctopamine, 4), a new β
Resonance Raman intensity analysis of the excited-state proton transfer in 2-hydroxyacetophenone.
Peteanu LA and Mathies RA.
The Journal of Physical Chemistry, 96(17), 6910-6916 (1992)
Na Li et al.
Molecules (Basel, Switzerland), 25(14) (2020-07-28)
Fluorophores with aggregation-induced emission enhancement (AIEE) characteristics applied in bioimaging have attracted more and more attention in recent years. In this work, a series of flavanone compounds with AIEE characteristics was developed and applied to fluorescence imaging of mitochondria and
A stereochemically well-defined rhodium (III) catalyst for asymmetric transfer hydrogenation of ketones
Matharu DS, et al.
Organic Letters, 7(24), 5489-5491 (2005)

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