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117374

Sigma-Aldrich

4′-Methoxyacetophenone

99%

Synonym(s):

4-Acetylanisole

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About This Item

Linear Formula:
CH3OC6H4COCH3
CAS Number:
100-06-1
Molecular Weight:
150.17
Beilstein/REAXYS Number:
742313
EC Number:
202-815-9
MDL number:
MFCD00008745
UNSPSC Code:
12352100
eCl@ss:
39023808
PubChem Substance ID:
24847327
NACRES:
NA.22

assay

99%

form

solid

bp

152-154 °C/26 mmHg (lit.)

mp

36-38 °C (lit.)

solubility

H2O: soluble 2.474 g/L at 20 °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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General description

4′-Methoxyacetophenone undergoes biocatalytic enantioselective reduction using immobilized Rhodotorula sp. AS2.2241 cells to yield (S)-1-(4-methoxyphenyl) ethanol in a hydrophilic ionic liquid-containing co-solvent system.

Application

4′-Methoxyacetophenone was used to study ruthenium catalyzed step growth copolymerization of 4′-methoxyacetophenone with α,ω-dienes to yield copolymers. It was used to determine the activity of various ketones approved as food additives against Clostridium Botulinum spores and cells.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

280.4 °F - open cup

flash_point_c

138 °C - open cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Ruthenium catalyzed regioselective step-growth copolymerization of 4'-methoxyacetophenone, or 4'-phenoxyacetophenone and a, ?-dienes.
Guo H and Weber WP.
Polym. Bull., 35(3), 259-264 (1995)
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
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))
[Toxicological characteristics of acetylanisole].
M I Makaruk et al.
Gigiena i sanitariia, (4)(4), 86-87 (1985-04-01)
Antibotulinal properties of selected aromatic and aliphatic ketones.
Bowles BL and Miller AJ.
Journal of Food Protection, 56(9), 795-800 (1993)
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