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137152-08-0

137152-08-0

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137152-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137152-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,1,5 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 137152-08:
(8*1)+(7*3)+(6*7)+(5*1)+(4*5)+(3*2)+(2*0)+(1*8)=110
110 % 10 = 0
So 137152-08-0 is a valid CAS Registry Number.

137152-08-0SDS

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 2-(4-chlorophenyl)-1-phenylsulfonylaziridine

1.2 Other means of identification

Product number -
Other names -

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:137152-08-0 SDS

137152-08-0Relevant articles and documents

A convenient method for the synthesis of 2-arylaziridines from styrene derivatives via 2-arylethenyl(diphenyl)sulfonium salts

Matsuo, Jun-Ichi,Yamanaka, Hiroyuki,Kawana, Asahi,Mukaiyama, Teruaki

, p. 392 - 393 (2003)

Styrene derivatives reacted with diphenyl(trifluoromethanesulfonyloxy)sulfonium trifluoromethanesulfonate (1) at low temperature to afford 2-arylethenyl(diphenyl)sulfonium triflates (2). Treatment of 2 with primary amines gave the corresponding 2-arylazir

Methylene Transfer from Dimethyloxosulphonium Methylide to N-Arylsulphonylaziridines: Stereospecific Synthesis of N-Arylsulphonylazetidines

Nadir, Upender K.,Sharma, Ms. Raman L.,Koul, Veerinder K.

, p. 2015 - 2020 (2007/10/02)

Several 2-alkyl, 2-aryl-, 2-benzyl-, 2,3-dialkyl- and 2,3-diarylsulphonylazetidines have been prepared in fair to good isolated yields through reaction of N-arylsulphonylaziridines with dimethyloxosulphonium methylide.Fused azetidines, however, could not

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