Cas 207281-67-2,2-[(2-Chloro-2-phenyl-acetyl)-(4-methoxy-benzyl)-amino]-acrylic acid methyl ester

207281-67-2

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Basic information

Product Name: 2-[(2-Chloro-2-phenyl-acetyl)-(4-methoxy-benzyl)-amino]-acrylic acid methyl ester
Synonyms: 2-[(2-Chloro-2-phenyl-acetyl)-(4-methoxy-benzyl)-amino]-acrylic acid methyl ester
CAS NO:207281-67-2
Molecular Formula:
Molecular Weight: 373.836
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-[(2-Chloro-2-phenyl-acetyl)-(4-methoxy-benzyl)-amino]-acrylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[(2-Chloro-2-phenyl-acetyl)-(4-methoxy-benzyl)-amino]-acrylic acid methyl ester(207281-67-2)
EPA Substance Registry System: 2-[(2-Chloro-2-phenyl-acetyl)-(4-methoxy-benzyl)-amino]-acrylic acid methyl ester(207281-67-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 207281-67-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 207281-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,2,8 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 207281-67:
(8*2)+(7*0)+(6*7)+(5*2)+(4*8)+(3*1)+(2*6)+(1*7)=122
122 % 10 = 2
So 207281-67-2 is a valid CAS Registry Number.

207281-67-2Upstream product

207281-67-2Downstream Products

207281-70-7 1-(4-Methoxy-benzyl)-5-oxo-4-phenyl-pyrrolidine-2-carboxylic acid methyl ester

207281-67-2Relevant academic research and scientific papers

Radical reactions leading to substituted pyroglutamates

Baker, S. Richard,Parsons, Andrew F.,Wilson, Michelle

, p. 2815 - 2818 (1998)

The Bu3SnH mediated cyclisation of a serine-derived dehydroalanine was shown to provide an efficient approach to a protected 4-phenylpyroglutamate which was elaborated to 4-phenylglutamic acid in good yield. Cyclisation reactions of this type w

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