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2-Azetidinecarbonitrile, 3-phenyl-1-(phenylmethyl)-, (2S,3R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

452096-22-9

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452096-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 452096-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,2,0,9 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 452096-22:
(8*4)+(7*5)+(6*2)+(5*0)+(4*9)+(3*6)+(2*2)+(1*2)=139
139 % 10 = 9
So 452096-22-9 is a valid CAS Registry Number.

452096-22-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3R)-1-benzyl-3-phenylazetidine-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-Azetidinecarbonitrile,3-phenyl-1-(phenylmethyl)-,(2S,3R)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:452096-22-9 SDS

452096-22-9Relevant academic research and scientific papers

A straightforward synthesis of enantiopure 2-cyano azetidines from β-amino alcohols

Agami, Claude,Couty, Francois,Evano, Gwilherm

, p. 297 - 302 (2007/10/03)

Enantiopure 2-cyano azetidines were prepared in high yields from β-amino alcohols. This synthesis was shown to be general and is based on two important steps: (i) chlorination of a N-cyanomethylated β-amino alcohol and (ii) a 4-exo-trig ring closure through the alkylation of a lithiated α-amino nitrile. The former step is stereoselective when ephedrine-derived β-amino alcohols are used. In the case of a phenylglycinol-derived β-amino alcohol, this step also involves a rearrangement.

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