Cas 373640-36-9,2-Bromo-2-[5-oxo-1-((R)-1-phenyl-ethyl)-pyrrolidin-2-yl]-propionic acid methyl ester

373640-36-9

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Basic information

Product Name: 2-Bromo-2-[5-oxo-1-((R)-1-phenyl-ethyl)-pyrrolidin-2-yl]-propionic acid methyl ester
Synonyms: 2-Bromo-2-[5-oxo-1-((R)-1-phenyl-ethyl)-pyrrolidin-2-yl]-propionic acid methyl ester
CAS NO:373640-36-9
Molecular Formula:
Molecular Weight: 354.244
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-Bromo-2-[5-oxo-1-((R)-1-phenyl-ethyl)-pyrrolidin-2-yl]-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Bromo-2-[5-oxo-1-((R)-1-phenyl-ethyl)-pyrrolidin-2-yl]-propionic acid methyl ester(373640-36-9)
EPA Substance Registry System: 2-Bromo-2-[5-oxo-1-((R)-1-phenyl-ethyl)-pyrrolidin-2-yl]-propionic acid methyl ester(373640-36-9)

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: 373640-36-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 373640-36-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,3,6,4 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 373640-36:
(8*3)+(7*7)+(6*3)+(5*6)+(4*4)+(3*0)+(2*3)+(1*6)=149
149 % 10 = 9
So 373640-36-9 is a valid CAS Registry Number.

373640-36-9Upstream product

373640-36-9Downstream Products

373640-36-9Relevant academic research and scientific papers

Influence of N-substituted lactams on acyclic free radical based hydrogen transfer

Guindon, Yvan,Bencheqroun, Mohammed

, p. 6041 - 6044 (2007/10/03)

anti Relative stereochemistry is achieved in the hydrogen-transfer reaction of a lactam adjacent to the carbon-centered radical. The sense of diastereoselectivity is reversed using N-substituted lactams, and optimal results favoring syn reduced products are obtained with an α-methylbenzyl group and a Boc group.

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