Cas 212699-53-1,(S)-N,N-dibenzyl-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxamide

212699-53-1

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Basic information

Product Name: (S)-N,N-dibenzyl-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxamide
Synonyms: (S)-N,N-dibenzyl-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxamide
CAS NO:212699-53-1
Molecular Formula:
Molecular Weight: 394.514
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)-N,N-dibenzyl-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N,N-dibenzyl-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxamide(212699-53-1)
EPA Substance Registry System: (S)-N,N-dibenzyl-1-(tert-butoxycarbonyl)-2-pyrrolidinecarboxamide(212699-53-1)

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: 212699-53-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 212699-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,6,9 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 212699-53:
(8*2)+(7*1)+(6*2)+(5*6)+(4*9)+(3*9)+(2*5)+(1*3)=141
141 % 10 = 1
So 212699-53-1 is a valid CAS Registry Number.

212699-53-1Upstream product

212699-53-1Downstream Products

212699-58-6 (S)-N,N-dibenzyl-2-pyrrolidinecarboxamide

212699-53-1Relevant academic research and scientific papers

Cyclopropane-Annelated Azaoligoheterocycles by Ti-Mediated Intramolecular Reductive Cyclopropanation of Cyclic Amino Acid Amides

Gensini, Martina,De Meijere, Armin

, p. 785 - 790 (2004)

Starting from pyrrole- and indole-2-carboxylic acids 5a and 5b, the tri- and tetracyclic N,N-dibenzylcyclopropylamines 7a and 7b have been synthesized in 52 and 33% overall yield, respectively. The synthesis of the enantiopure tetracyclic diamine 10 has b

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