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Merck
CN

117374

4′-Methoxyacetophenone

99%

Synonym(s):

4-Acetylanisole

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About This Item

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

4′-Methoxyacetophenone, 99%

InChI key

NTPLXRHDUXRPNE-UHFFFAOYSA-N

InChI

1S/C9H10O2/c1-7(10)8-3-5-9(11-2)6-4-8/h3-6H,1-2H3

SMILES string

COc1ccc(cc1)C(C)=O

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

functional group

ketone

Quality Level

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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.

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.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

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


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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)
Antibotulinal properties of selected aromatic and aliphatic ketones.
Bowles BL and Miller AJ.
Journal of Food Protection, 56(9), 795-800 (1993)
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)
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

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