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71556-64-4

71556-64-4

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71556-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71556-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,5 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71556-64:
(7*7)+(6*1)+(5*5)+(4*5)+(3*6)+(2*6)+(1*4)=134
134 % 10 = 4
So 71556-64-4 is a valid CAS Registry Number.

71556-64-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-benzhydrylazetidine-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 1-benzhydryl-2-azetidinyl carboxylate

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:71556-64-4 SDS

71556-64-4Relevant articles and documents

Synthesis of 2-phenyl- and 2,2-diarylpyrrolidines through Stevens rearrangement performed on azetidinium ions

Drouillat, Bruno,D'Aboville, Edouard,Bourdreux, Flavien,Couty, Francois

supporting information, p. 1103 - 1109 (2014/03/21)

A set of azetidinium ions substituted at the nitrogen atom either by a benzyl group or a benzhydryl group were synthesized to delineate the scope of their ring expansion into 2-phenyl- or 2,2-diaryl-pyrrolidines through a Stevens rearrangement. Whereas th

Synthesis and structure-activity relationships of aminoalkylazetidines as ORL1 receptor ligands

Wu, Wen-Lian,Caplen, Mary Ann,Domalski, Martin S.,Zhang, Hongtao,Fawzi, Ahmad,Burnett, Duane A.

, p. 3157 - 3160 (2007/10/03)

A series of aminoalkylazetidines has been discovered as novel ORL1 receptor ligands. Structure-activity relationships have been investigated at the azetidine N and the alkyl side chain sites. Several potent and selective analogues have been identified.

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