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Ethyl 2-acetyl-2-benzyl-4-oxo-4-phenylbutanoate is a complex organic compound with the molecular formula C20H20O4. It is a derivative of butanoic acid, featuring a 4-phenylbutanoate structure with an acetyl group at the 2-position and a benzyl group at the same position, forming a ketone. ethyl 2-acetyl-2-benzyl-4-oxo-4-phenylbutanoate is characterized by its ester functionality, with an ethyl group attached to the carboxylic acid moiety. It is a colorless to pale yellow solid and is soluble in organic solvents. Ethyl 2-acetyl-2-benzyl-4-oxo-4-phenylbutanoate is synthesized through a series of chemical reactions and is used in the pharmaceutical industry, particularly as an intermediate in the synthesis of certain drugs. Its chemical structure and properties make it a valuable compound for further research and development in medicinal chemistry.

6938-63-2

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6938-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6938-63-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,3 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6938-63:
(6*6)+(5*9)+(4*3)+(3*8)+(2*6)+(1*3)=132
132 % 10 = 2
So 6938-63-2 is a valid CAS Registry Number.

6938-63-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-acetyl-2-benzyl-4-oxo-4-phenylbutanoate

1.2 Other means of identification

Product number -
Other names ethyl 2-acetyl-2-benzyl-4-oxo-4-phenylbutyrate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:6938-63-2 SDS

6938-63-2Relevant academic research and scientific papers

Cerium-catalyzed, aerobic oxidative synthesis of 1,2-dioxane derivatives from styrene and their fragmentation into 1,4-dicarbonyl compounds

Roessle, Michael,Werner, Thomas,Frey, Wolfgang,Christoffers, Jens

, p. 5031 - 5038 (2007/10/03)

1,4-Diketones were prepared by cerium-catalyzed oxidative coupling of styrene with molecular oxygen and 1,3-dicarbonyl compounds. This two-step sequence was performed as a one-pot procedure without isolation of the intermediate products. The first step is

PHOTOCHEMISTRY OF SUBSTITUTED CYCLIC ENONES. PART 6. PHOTOCHEMICAL REACTIONS OF 5-ARYLMETHYL-3-PHENYLCYCLOPENT-2-ENONES. A PHOTOSTATIONARY STATE1,2

Clements, Michael T.,McMurry, Brian H.

, p. 1810 - 1813 (2007/10/02)

Photolysis of 5-(1-and 2-naphtylmethyl)-3-phenylcyclopent-2-enones affords cycloaddition products, the 7,8- and 5,6-benzo-fused 10-phenyltetracyclo3,10.04,9>dodeca-5,7-dien-2-ones respectively, in equilibrium with the

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