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41369-60-2

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41369-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41369-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,6 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41369-60:
(7*4)+(6*1)+(5*3)+(4*6)+(3*9)+(2*6)+(1*0)=112
112 % 10 = 2
So 41369-60-2 is a valid CAS Registry Number.

41369-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(p-toluenesulfonylmethyl)-p-toluenesulfonamide

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:41369-60-2 SDS

41369-60-2Relevant articles and documents

Photoredox-Catalyzed Intramolecular Aminodifluoromethylation of Unactivated Alkenes

Zhang, Zuxiao,Tang, Xiaojun,Thomoson, Charles S.,Dolbier, William R.

supporting information, p. 3528 - 3531 (2015/07/28)

A photoredox catalyzed aminodifluoromethylation of unactivated alkenes has been developed in which HCF2SO2Cl is used as the HCF2 radical source. Sulfonamides were active nucleophiles in the final step of a tandem addition/oxidation/cyclization process to form pyrrolidines, and esters were found to cyclize to form lactones. Thus, a variety of pyrrolidines and lactones were obtained in moderate to excellent yield. In order for the cyclization reactions to be efficient, a combination of a copper catalyst (Cu(dap)2Cl) and silver carbonate was crucial to suppressing a competing chloro, difluoroalkylation process.

Highly selective palladium-catalyzed intramolecular chloroamination of unactivated alkenes by using hydrogen peroxide as an oxidant

Yin, Guoyin,Wu, Tao,Liu, Guosheng

supporting information; experimental part, p. 451 - 455 (2012/02/15)

Cheap and clean! A novel Pd-catalyzed oxidative intramolecular chloroamination of unactivated alkenes has been developed by using hydrogen peroxide as an oxidant and CaCl2 as a chlorine source. A series of chlorinated piperidine derivatives has

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