64710
4′-Methoxyacetophenone
purum, ≥99.0% (GC)
Synonym(s):
4-Acetylanisole
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About This Item
Linear Formula:
CH3OC6H4COCH3
CAS Number:
Molecular Weight:
150.17
Beilstein/REAXYS Number:
742313
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
grade
purum
assay
≥99.0% (GC)
form
solid
bp
152-154 °C/26 mmHg (lit.)
mp
36-38 °C (lit.)
37-39 °C
SMILES string
COc1ccc(cc1)C(C)=O
InChI
1S/C9H10O2/c1-7(10)8-3-5-9(11-2)6-4-8/h3-6H,1-2H3
InChI key
NTPLXRHDUXRPNE-UHFFFAOYSA-N
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[Toxicological characteristics of acetylanisole].
M I Makaruk et al.
Gigiena i sanitariia, (4)(4), 86-87 (1985-04-01)
Wen-Yong Lou et al.
Journal of biotechnology, 143(3), 190-197 (2009-07-21)
The biocatalytic enantioselective reduction of 4'-methoxyacetophenone to (S)-1-(4-methoxyphenyl)ethanol was successfully conducted in a hydrophilic IL-containing co-solvent system using immobilized Rhodotorula sp. AS2.2241 cells. Of all the tested ILs, the best results were observed with the novel IL 1-(2'-hydroxy)ethyl-3-methylimidazolium nitrate (C(2)OHMIM.NO(3))
Sanja Ćavar et al.
Pharmaceutical biology, 48(2), 170-176 (2010-07-22)
Stachys menthifolia Vis. (Lamiaceae) is an endemic species from the Balkan Peninsula spread throughout Albania, Greece, Montenegro, and Croatia. This article presents the first investigation of the essential oil composition of this species from Croatia. Aerial parts of the plant
Shakila K Evans et al.
Chemical biology & drug design, 75(3), 333-337 (2010-07-28)
Acetophenones were screened for activity against positive phototaxis of Chlamydomonas cells, a process that requires co-ordinated flagellar motility. The structure-activity relationships of a series of acetophenones are reported, including acetophenones that affect flagellar motility and cell viability. Notably, 4-methoxyacetophenone, 3,4-dimethoxyacetophenone
Shinya Tachibana et al.
Journal of oleo science, 57(2), 107-113 (2008-01-17)
The synthesis and physiological activity of thiophenes and furans with methoxyacetophenone derivatives were examined. 3-Methoxyacetophenone (1) and 4-methoxyacetophenone (2) were converted, respectively, to the oximes (3) and (4) by oximation with hydroxylamine hydrochloride, and to the primary amines (5) and
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