117374

Sigma-Aldrich

4′-Methoxyacetophenone

99%

Synonym(s):
4-Acetylanisole
Linear Formula:
CH3OC6H4COCH3
CAS Number:
Molecular Weight:
150.17
Beilstein/REAXYS Number:
742313
EC Number:
MDL number:
eCl@ss:
39023808
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

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.

Packaging

1 kg in poly bottle
5, 100 g in poly bottle

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

RIDADR

NONH for all modes of transport

WGK Germany

WGK 2

Flash Point(F)

280.4 °F - open cup

Flash Point(C)

138 °C - open cup

Certificate of Analysis

Certificate of Origin

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)
[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...

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