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Diethyl [(chloroacetyl)(phenyl)amino]propanedioate is a complex organic compound with the chemical formula C15H18ClNO5. It is a derivative of chloroacetyl chloride and phenylalanine, featuring a chloroacetyl group attached to a phenyl ring, which is further connected to a propanedioate moiety. diethyl [(chloroacetyl)(phenyl)amino]propanedioate is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain antibiotics and other bioactive molecules. Its structure allows for the formation of esters and amides, which can be further modified to create a range of chemical entities with different properties and uses. The compound's reactivity and versatility make it a valuable component in the field of organic chemistry and drug development.

5634-74-2

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5634-74-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5634-74-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5634-74:
(6*5)+(5*6)+(4*3)+(3*4)+(2*7)+(1*4)=102
102 % 10 = 2
So 5634-74-2 is a valid CAS Registry Number.

5634-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethyl (2-chloro-N-phenylacetamido)malonate

1.2 Other means of identification

Product number -
Other names N-Phenyl-chloracetamidomalonsaeurediaethylester

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 -
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More Details:5634-74-2 SDS

5634-74-2Relevant academic research and scientific papers

153. Azomalonate Syntheses; Part II; Synthesis and Reactivity of Novel 1,2,4-Triazin-5-one Derivatives

Heckendorn, Roland

, p. 1700 - 1718 (2007/10/02)

Base treatment of azomalonates derived from N-substituted dialkyl (2-chloroacetamido)malonates results in the formation of 4-substituted alkyl 5-oxo-1,4,5,6-tetrahydro-1,2,4-triazine-3-carboxylates.The same malonates coupled with diazotized 2-amino-5-chlo

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