H18607
2′-Hydroxyacetophenone
ReagentPlus®, 99%
Synonym(s):
2-Acetylphenol
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About This Item
Linear Formula:
HOC6H4COCH3
CAS Number:
Molecular Weight:
136.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-288-0
Beilstein/REAXYS Number:
386123
MDL number:
Assay:
99%
Form:
liquid
InChI
1S/C8H8O2/c1-6(9)7-4-2-3-5-8(7)10/h2-5,10H,1H3
InChI key
JECYUBVRTQDVAT-UHFFFAOYSA-N
SMILES string
CC(=O)c1ccccc1O
vapor density
4.7 (vs air)
vapor pressure
~0.2 mmHg ( 20 °C)
product line
ReagentPlus®
assay
99%
form
liquid
Quality Level
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.)
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Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
222.8 °F - closed cup
flash_point_c
106 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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
Subramanya Gupta Sreerama et al.
Inorganic chemistry, 44(18), 6299-6307 (2005-08-30)
A series of dinuclear complexes of Mn(III), Fe(III), and Co(III) with two diazine Schiff bases, H2salhn and H2mesalhn, is reported. The Schiff bases are prepared by condensation reactions of hydrazine with salicylaldehyde (H2salhn) and with 2-hydroxyacetophenone (H2mesalhn) in 1:2 mol
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, 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
José I Borrell et al.
Molecular diversity, 8(2), 147-157 (2004-06-24)
Two new solid-phase syntheses of substituted pyrazoles are described. The first includes supporting an o-hydroxyacetophenone on Merrifield resin, Vilsmeier-Haack formylation on the methyl group and cyclization with a substituted hydrazine to afford a pyrazole ring with two diversity centers. The
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