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31378-00-4

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31378-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31378-00-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,3,7 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31378-00:
(7*3)+(6*1)+(5*3)+(4*7)+(3*8)+(2*0)+(1*0)=94
94 % 10 = 4
So 31378-00-4 is a valid CAS Registry Number.

31378-00-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-4-[(4-nitrophenyl)methylsulfanylsulfonyl]benzene

1.2 Other means of identification

Product number -
Other names 4-Nitrobenzyl-p-toluolthiolsulfonat

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:31378-00-4 SDS

31378-00-4Relevant articles and documents

Design and synthesis of garlic-related unsymmetrical thiosulfonates as potential Alzheimer's disease therapeutics: In vitro and in silico study

Zilbeyaz, Kani,Oztekin, Aykut,Kutluana, Emine Gunbatar

, (2021/05/13)

Garlic contains a wide range of organosulfur compounds, which exhibit a broad spectrum of biological activities. Amongst the sulfur-containing compounds in garlic, the thiosulfonates are considerably popular in various fields. In light of this, we decided

Perfluoroalkylation of Thiosulfonates: Synthesis of Perfluoroalkyl Sulfides

Luo, Ziwei,Yang, Xinkan,Tsui, Gavin Chit

supporting information, p. 6155 - 6159 (2020/07/30)

A practical synthesis of perfluoroalkyl sulfides is described. The method employs stable and readily accessible thiosulfonates as new electrophiles with commercial nucleophilic perfluoroalkylating reagents. The mild reaction conditions allow access to a wide variety of both aryl- and alkyl-substituted perfluoroalkyl sulfides amenable to pharmaceutical development. Furthermore, the reaction operation is straightforward, odorless, does not produce toxic wastes, and, therefore should appeal to practitioners in industrial-scale productions.

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