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75898-95-2

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75898-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75898-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,9 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75898-95:
(7*7)+(6*5)+(5*8)+(4*9)+(3*8)+(2*9)+(1*5)=202
202 % 10 = 2
So 75898-95-2 is a valid CAS Registry Number.

75898-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-acetamido-3-(2-chloro-1,1-difluoroethyl)sulfanylpropanoic acid

1.2 Other means of identification

Product number -
Other names L-Cysteine,N-acetyl-S-(2-chloro-1,1-difluoroethyl)

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:75898-95-2 SDS

75898-95-2Downstream Products

75898-95-2Relevant articles and documents

Synthesis of Mercapturic Acids Related to the Metabolism of Halothane

Sachdev, Krishna G.,Cohen, Ellis N.,Cheung, H. T. Andrew,Chau, Dieu D.

, p. 2868 - 2883 (2007/10/02)

Mercapturic acid derivatives corresponding to possible or actual metabolites of the anaesthetic halothane (2-bromo-2-chloro-1,1,1-trifluoroethane) were synthesized by the reaction of N-acetyl-L-cysteine with 2-bromo-2-chloro-1,1-difluoroethene, 2-chloro-1,1-difluoroethene, and 2-bromo-1,1-difluoroethene.Saturated conjugates of the type RSCF2CHXY were formed by nucleophilic addition of the thiolate anion when the reaction was carried out in aqueous methanol containing sodium hydroxide.Unsaturated conjugates of the type RSCF=CHX, corresponding to displacement of fluorine, were the major products from the latter two alkenes under anhydrous aprotic conditions using N,N-dimethylformamide and triethylamine.Structure assignments of the conjugates are based mainly on 1H and 13C n.m.r. data.

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