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H18607

Sigma-Aldrich

2′-Hydroxyacetophenone

ReagentPlus®, 99%

Synonym(s):

2-Acetylphenol

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About This Item

Linear Formula:
HOC6H4COCH3
CAS Number:
118-93-4
Molecular Weight:
136.15
Beilstein:
386123
EC Number:
204-288-0
MDL number:
MFCD00002219
UNSPSC Code:
12352100
PubChem Substance ID:
24895486
NACRES:
NA.22

vapor density

4.7 (vs air)

vapor pressure

~0.2 mmHg ( 20 °C)

product line

ReagentPlus®

Assay

99%

form

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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Legal Information

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Nora H Al-Shaalan
Molecules (Basel, Switzerland), 16(10), 8629-8645 (2011-10-15)
The Schiff base hydrazone ligand HL was prepared by the condensation reaction of 7-chloro-4-quinoline with o-hydroxyacetophenone. The ligand behaves either as monobasic bidentate or dibasic tridentate and contain ONN coordination sites. This was accounted for be the presence in the
Mohammed Y Merza et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(7), 1677-1683 (2004-05-19)
Ultra violet absorption spectra of o-methylacetophenone, o-fluoroacetophenone and o-hydroxyacetophenone solutions in different solvents are recorded in the region 200-350 nm at room temperature. Excited state dipole moments for three (pi* <-- pi) transitions of the benzene ring for solutions in
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
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
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