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Ethyl 2-oxo-3,3-diphenylpropanoate is a chemical compound with the molecular formula C17H16O3. It is an organic ester derived from the carboxylic acid 2-oxo-3,3-diphenylpropanoic acid and ethanol. ethyl 2-oxo-3,3-diphenylpropanoate is characterized by its aromatic structure, featuring two phenyl rings attached to a central carbonyl group, which is in turn connected to an ethyl ester group. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and other organic compounds due to its unique structure and reactivity. The compound is also known for its potential applications in the development of new materials and as an intermediate in the production of certain drugs.

6362-64-7

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6362-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6362-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6362-64:
(6*6)+(5*3)+(4*6)+(3*2)+(2*6)+(1*4)=97
97 % 10 = 7
So 6362-64-7 is a valid CAS Registry Number.

6362-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-oxo-3,3-diphenylpropanoate

1.2 Other means of identification

Product number -
Other names Diphenyl-brenztraubensaeure-aethylester

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6362-64-7 SDS

6362-64-7Relevant academic research and scientific papers

Pyruvate enolate arylation and alkylation: OBO ester protected pyruvates as useful reagents in organic synthesis

Henrique Alves Esteves,Hall, Christopher J. J.,Smith, Peter D.,Donohoe, Timothy J.

supporting information, p. 5248 - 5251 (2017/11/06)

A protected pyruvate equivalent is described that allows arylation and arylation/alkylation reactions to be performed at the methyl group. Utilization of the OBO derivative of the pyruvate ester allowed the application of palladium catalyzed arylation reactions together with subsequent alkylation, under basic conditions. Moreover, the OBO protecting group could be easily removed in one step to provide access to a wide range of substituted pyruvate derivatives.

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