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85195-24-0

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85195-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85195-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,9 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 85195-24:
(7*8)+(6*5)+(5*1)+(4*9)+(3*5)+(2*2)+(1*4)=150
150 % 10 = 0
So 85195-24-0 is a valid CAS Registry Number.

85195-24-0SDS

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 methyl 2-(benzylsulfonylamino)-2-oxoacetate

1.2 Other means of identification

Product number -
Other names methyl N-(benzylsulfonyl)oxamate

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:85195-24-0 SDS

85195-24-0Relevant articles and documents

Methyl N-(benzylsulfonyl)oxamate as a probable intermediate in the synthesis of 4-hydroxy-5-phenyl-3(2H)-isothiazolone 1,1-dioxide from phenylmethanesulfamide and dimethyl oxalate in the presence of bases

Zlotin, S. G.,Gerasyuto, A. I.

, p. 394 - 395 (1999)

The formation of 4-hydroxy-5-phenyl-3(2H)-isothiazolone 1,1-dioxide from phenylmethanesulfamide and dimethyl oxalate under the action of bases is apparently a two-stage process involving the formation of linear methyl N-(benzylsulfonyl)oxamate followed by

5-Aryl-4-hydroxy-3(2H)-isothiazolone 1,1-Dioxide Derivatives. Synthesis and 13C NMR Characterization

Rooney, C. S.,Cochran, D. W.,Ziegler, C.,Cragoe, E. J.,Williams, H. W. R.

, p. 2212 - 2217 (2007/10/02)

5-Phenyl- and 5-thiazolyl-4-hydroxy-3(2H)-isothiazolone 1,1-dioxide derivatives have been prepared by base-catalyzed cyclocondensation of diethyl oxalate with an arylmethanesulfonamide, as well as by reaction of an arylmethanesulfonamide with methyl or et

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