Cas 220329-92-0,(S)-2-[(R)-1-((R)-1-Benzyloxy-2-oxo-2-pyrrolidin-1-yl-ethyl)-allyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

220329-92-0

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Basic information

Product Name: (S)-2-[(R)-1-((R)-1-Benzyloxy-2-oxo-2-pyrrolidin-1-yl-ethyl)-allyl]-pyrrolidine-1-carboxylic acid tert-butyl ester
Synonyms: (S)-2-[(R)-1-((R)-1-Benzyloxy-2-oxo-2-pyrrolidin-1-yl-ethyl)-allyl]-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS NO:220329-92-0
Molecular Formula:
Molecular Weight: 428.572
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: (S)-2-[(R)-1-((R)-1-Benzyloxy-2-oxo-2-pyrrolidin-1-yl-ethyl)-allyl]-pyrrolidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(R)-1-((R)-1-Benzyloxy-2-oxo-2-pyrrolidin-1-yl-ethyl)-allyl]-pyrrolidine-1-carboxylic acid tert-butyl ester(220329-92-0)
EPA Substance Registry System: (S)-2-[(R)-1-((R)-1-Benzyloxy-2-oxo-2-pyrrolidin-1-yl-ethyl)-allyl]-pyrrolidine-1-carboxylic acid tert-butyl ester(220329-92-0)

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: 220329-92-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220329-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,3,2 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 220329-92:
(8*2)+(7*2)+(6*0)+(5*3)+(4*2)+(3*9)+(2*9)+(1*2)=100
100 % 10 = 0
So 220329-92-0 is a valid CAS Registry Number.

220329-92-0Upstream product

220329-92-0Downstream Products

154221-22-4 (1R,2R,7aS)-2-Benzyloxy-1-vinyl-hexahydro-pyrrolizin-3-one

220329-92-0Relevant academic research and scientific papers

Zwitterionic aza-Claisen rearrangement: Reaction of carboxylic acid fluorides with N-allyl amines

Laabs, Stephan,Scherrmann, Andreas,Sudau, Alexander,Diederich, Michel,Kierig, Camilla,Nubbemeyer, Udo

, p. 25 - 28 (2007/10/03)

A significant yield enhancement is observed by replacing carboxylic acid chlorides by the corresponding fluorides in the zwitterionic aza-Claisen rearrangement of N-allyl amines. The von Braun type degradation as the major competing reaction involving the

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