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75457-08-8

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75457-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75457-08-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,5 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75457-08:
(7*7)+(6*5)+(5*4)+(4*5)+(3*7)+(2*0)+(1*8)=148
148 % 10 = 8
So 75457-08-8 is a valid CAS Registry Number.

75457-08-8SDS

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 N-(2,2,2-trichloro-1-hydroxyethyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names D138

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:75457-08-8 SDS

75457-08-8Relevant articles and documents

New approach to the preparation of p-(1-cyanoethyl)arenesulfonamides by reaction of arylsulfonyl imines of polychloroacetaldehydes with acetone cyanohydrin

Kaliev,Serykh, V. Yu.,Rosentsveig

, p. 1191 - 1194 (2017/09/29)

Reaction of N-(2,2,2-trichloroethylidene)- or N-(1-phenyl-2,2-dichloroethylidene)arenesulfonamides with acetone cyanohydrin in acetone in the presence of potassium carbonate led to the formation of N- (2,2,2-trichloro-1-cyanoethyl)- or N-(2-phenyl-2,2-dic

Transformations of N-(2,2,2-Trichloroethylidene)-arenesulfonamides

Drozdova,Mirskova

, p. 1330 - 1336 (2007/10/03)

N-(2,2,2-Trichloroethylidene)arenesulfonamides take up at the double C=N bond benzyl and 2-propynyl alcohols and aromatic and unsaturated aliphatic carboxylic acids to give N-(2,2,2-trichloroethyl)-arenesulfonamides. Reactions of the title compounds with dibasic acids (oxalic, succinic, and adipic) result in formation of 1:1 and 2:1 addition products.

TRICHLOROETHYLIDENEARENESULFONAMIDES IN REACTION WITH FURAN AND ITS DERIVATIVES

Levkovskaya, G. G.,Evstaf'eva, I. T.,Mirskova, A. N.,Zhuravlev, S. N.,Kul'nevich, V. G.

, p. 1762 - 1765 (2007/10/02)

Trichloroethylidenearenesulfonamides enter into reaction with furan and 2-methylfuran without a catalyst, forming the previously unknown N-ethyl- and N-ethylarenesulfonamides; the reaction does not go with 2-

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