Cas 797039-63-5,[(S)-1-((2R,3R)-1-Benzyl-3-phenyl-azetidin-2-yl)-ethyl]-carbamic acid tert-butyl ester

797039-63-5

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Basic information

Product Name: [(S)-1-((2R,3R)-1-Benzyl-3-phenyl-azetidin-2-yl)-ethyl]-carbamic acid tert-butyl ester
Synonyms: [(S)-1-((2R,3R)-1-Benzyl-3-phenyl-azetidin-2-yl)-ethyl]-carbamic acid tert-butyl ester
CAS NO:797039-63-5
Molecular Formula:
Molecular Weight: 366.503
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)-1-((2R,3R)-1-Benzyl-3-phenyl-azetidin-2-yl)-ethyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-1-((2R,3R)-1-Benzyl-3-phenyl-azetidin-2-yl)-ethyl]-carbamic acid tert-butyl ester(797039-63-5)
EPA Substance Registry System: [(S)-1-((2R,3R)-1-Benzyl-3-phenyl-azetidin-2-yl)-ethyl]-carbamic acid tert-butyl ester(797039-63-5)

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: 797039-63-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 797039-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,7,0,3 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 797039-63:
(8*7)+(7*9)+(6*7)+(5*0)+(4*3)+(3*9)+(2*6)+(1*3)=215
215 % 10 = 5
So 797039-63-5 is a valid CAS Registry Number.

797039-63-5Upstream product

797039-63-5Downstream Products

797039-63-5Relevant academic research and scientific papers

General route to a new class of homochiral azetidine-derived 1,2 diamines

Couty, Francois,Evano, Gwilherm,Prim, Damien,Marrot, Jerome

, p. 3893 - 3897 (2007/10/03)

A short access to novel azetidine-derived anti-1,2-diamines starting from easily accessible 2-cyanoazetidines has been developed. A one-pot sequence, including a nucleophilic addition and reduction of the resulting imine, allows for a dia-stereoselective synthesis of variously substituted diamines. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

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