Skip to Content
Merck
All Photos(1)

Documents

199176

Sigma-Aldrich

4-Methoxyphenylacetone

≥97%

Synonym(s):

4-Methoxybenzyl methyl ketone

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3OC6H4CH2COCH3
CAS Number:
122-84-9
Molecular Weight:
164.20
Beilstein:
2044332
EC Number:
204-578-7
MDL number:
MFCD00008773
UNSPSC Code:
12352100
PubChem Substance ID:
24851896
NACRES:
NA.22

Quality Level

200

Assay

≥97%

form

liquid

refractive index

n20/D 1.525 (lit.)

bp

145 °C/25 mmHg (lit.)

density

1.067 g/mL at 25 °C (lit.)

SMILES string

COc1ccc(CC(C)=O)cc1

InChI

1S/C10H12O2/c1-8(11)7-9-3-5-10(12-2)6-4-9/h3-6H,7H2,1-2H3

InChI key

WFWKNGZODAOLEO-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Asymmetric amination of 4-methoxyphenylacetone was studied.

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

215.6 °F - closed cup

Flash Point(C)

102 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Asymmetric amination of 4-methoxyphenylacetone and its related compounds with microorganisms.
Applied Microbiology and Biotechnology, 33(6), 637-640 (1990)
Hamid Sadeghian et al.
Bioorganic & medicinal chemistry, 17(6), 2327-2335 (2009-03-03)
A group of 4-methoxyphenylacetic acid esters were designed, synthesized and evaluated as potential inhibitors of soybean 15-lipoxygenase (SLO) on the basis of eugenol and esteragol structures. Compounds 7d-e showed the best IC(50) in SLO inhibition (IC(50)=3.8 and 1.9 microM, respectively).

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service