Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

544302

Sigma-Aldrich

Methyl 4-acetylbenzoate

98%

Sign Into View Organizational & Contract Pricing

Synonym(s):
4-Acetobenzoic acid methyl ester
Linear Formula:
CH3COC6H4CO2CH3
CAS Number:
Molecular Weight:
178.18
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

mp

93-96 °C (lit.)

SMILES string

COC(=O)c1ccc(cc1)C(C)=O

InChI

1S/C10H10O3/c1-7(11)8-3-5-9(6-4-8)10(12)13-2/h3-6H,1-2H3

InChI key

QNTSFZXGLAHYLC-UHFFFAOYSA-N

General description

Methyl 4-acetylbenzoate is an aromatic ketone that can be prepared from 4-bromoacetophenone.

Application

Methyl 4-acetylbenzoate may be used in the preparation of 4-methoxycarbonyl-α-oxo-benzeneacetic acid and methyl 4-(2-(2-methylimidazo[1,2-a]pyridin-3-yl)-2-oxoacetyl)benzoate.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

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

Regioselective Copper?Catalyzed Oxidative Cross?Coupling of Imidazo [1,2?a] pyridines with Methyl Ketones: An Efficient Route for Synthesis of 1,2?Diketones.
Lei S, et al.
Advanced Bacterial Genetics, Cold Spring Harbor, 358(1), 67-73 (2016)
Enantioselective photochemical synthesis of a ?-lactam via the solid state ionic chiral auxiliary method.
Scheffer JR and Wang K.
Synthesis, 112(08), 1253-1257 (2001)

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