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Ethyl (2-methylbenzoyl)acetate_Molecular_structure_CAS_51725-82-7)
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Ethyl (2-methylbenzoyl)acetate

Catalog No. 559148 Name Sigma Aldrich
CAS Number 51725-82-7 Website http://www.sigmaaldrich.com
M. F. C12H14O3 Telephone 1-800-521-8956
M. W. 206.23776 Fax
Purity 97% Email
Storage Chembase ID: 152844

SYNONYMS

Title
(2-甲基苯甲酰)乙酸乙酯
IUPAC name
ethyl 3-(2-methylphenyl)-3-oxopropanoate
IUPAC Traditional name
ethyl 3-(2-methylphenyl)-3-oxopropanoate
Synonyms
Ethyl 2-(2-methylbenzoyl)acetate
Ethyl o-methylbenzoylacetate
Ethyl o-toluoylacetate
Ethyl 3-(2-methylphenyl)-3-oxopropanoate
Ethyl 3-oxo-3-(o-tolyl)propanoate

DATABASE IDS

PubChem SID 24879799
CAS Number 51725-82-7
MDL Number MFCD03424817

PROPERTIES

Linear Formula CH3C6H4COCH2CO2CH2CH3
Purity 97%
Boiling Point 256-257 °C(lit.)
Density 1.069 g/mL at 25 °C(lit.)
Refractive Index n20/D 1.5255(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves
German water hazard class 3

DETAILS

Description (English)
Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Preparation of highly substituted furans by tandem condensation-cyclization reactions using bismuth triflate catalyst1
• Co/Mn-mediated oxidative cross-coupling2
• Enantioselective ruthenium-catalyzed hydrogenation3
• Preparation of cambinol analogs for sirtuin inhibition with antitumor action4
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Reactant for:
• Preparation of highly substituted furans by tandem condensation-cyclization reactions using bismuth triflate catalyst1
• Co/Mn-mediated oxidative cross-coupling2
• Enantioselective ruthenium-catalyzed hydrogenation3
• Preparation of cambinol analogs for sirtuin inhibition with antitumor action4

REFERENCES