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Methyl 3-(diphenylamino)-3-oxo-2-phenylpropanoate is a complex organic compound with the chemical formula C23H21NO3. It is a derivative of phenylalanine, an essential amino acid, and features a diphenylamino group attached to the 3-position of the propanoate chain. This molecule is characterized by its ester functionality, with a methyl group attached to the carboxylic acid group, and a ketone group at the 3-position. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structure and reactivity. The compound's properties, such as its solubility and stability, make it a valuable building block in organic chemistry and drug development.

6636-17-5

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6636-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6636-17-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6636-17:
(6*6)+(5*6)+(4*3)+(3*6)+(2*1)+(1*7)=105
105 % 10 = 5
So 6636-17-5 is a valid CAS Registry Number.

6636-17-5SDS

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 methyl 3-oxo-2-phenyl-3-(N-phenylanilino)propanoate

1.2 Other means of identification

Product number -
Other names methyl 3-(diphenylamino)-3-oxo-2-phenylpropanoate

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:6636-17-5 SDS

6636-17-5Relevant academic research and scientific papers

Cascade Formation of C3-Unsymmetric Spirooxindoles via PhI(OAc)2-Mediated Oxidative C?C/C?N Bond Formation

Sun, Jiyun,Li, Guangchen,Zhang, Guangtao,Cong, Ying,An, Xuechan,Zhang-Negrerie, Daisy,Du, Yunfei

, p. 2476 - 2481 (2018/05/30)

A series of C3-unsymmetric spirooxindoles were achieved by reaction of diphenylmalonamides with PhI(OAc)2 (PIDA) under metal-free conditions. Control experiments suggest that the hypervalent iodine-mediated reaction undergoes a cascade process involving an oxidative C?C bond formation preceeding an oxidative C?N bond formation. (Figure presented.).

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