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10405-52-4

10405-52-4

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  • Benzenesulfonamide,4-methyl-N-[1-methyl-2-[[(4-methylphenyl)sulfonyl]oxy]-1-[[[(4-methylphenyl)sulfonyl]oxy]methyl]ethyl]-

    Cas No: 10405-52-4

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  • Benzenesulfonamide,4-methyl-N-[1-methyl-2-[[(4-methylphenyl)sulfonyl]oxy]-1-[[[(4-methylphenyl)sulfonyl]oxy]methyl]ethyl]- cas 10405-52-4

    Cas No: 10405-52-4

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10405-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10405-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,0 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10405-52:
(7*1)+(6*0)+(5*4)+(4*0)+(3*5)+(2*5)+(1*2)=54
54 % 10 = 4
So 10405-52-4 is a valid CAS Registry Number.

10405-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-methyl-2-[(4-methylphenyl)sulfonylamino]-3-(4-methylphenyl)sulfonyloxypropyl] 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names N-(1,1-bis(hydroxymethyl)ethyl)-p-toluenesulfonamide,di-p-toluenesulfonate

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:10405-52-4 SDS

10405-52-4Relevant articles and documents

Tetrathiomolybdate mediated rearrangement of aziridinemethanol tosylates: A thia-aza-payne rearrangement

Sureshkumar, Devarajulu,Koutha, Srinivasamurthy,Ganesh, Venkataraman,Chandrasekaran, Srinivasan

experimental part, p. 5533 - 5541 (2010/11/04)

Aziridinemethanol sulfonate esters react with tetrathiomolybdate 1 to give thiirane derivatives as the major product and cyclic disulfides as minor product under mild reaction conditions via an unprecedented thia-aza-Payne-type rearrangement. Interestingly, when the reaction of 1 was carried out with 2-aziridino-cyclohexanol derivatives it resulted in the formation of thia-bicyclo[3.1.1]heptane or dithia-bicyclo[3.2.1]octane derivatives.

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