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5-broMothiophene-2-sulfinic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73348-44-4

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73348-44-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73348-44-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,4 and 8 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73348-44:
(7*7)+(6*3)+(5*3)+(4*4)+(3*8)+(2*4)+(1*4)=134
134 % 10 = 4
So 73348-44-4 is a valid CAS Registry Number.

73348-44-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromothiophene-2-sulfonic acid

1.2 Other means of identification

Product number -
Other names 5-bromo-thiophene-2-sulfonic acid

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:73348-44-4 SDS

73348-44-4Relevant academic research and scientific papers

STUDY OF KINETICS AND MECHANISM OF SULFONATION OF THIOPHENE AND ITS DERIVATIVES BY COMPLEX COMPOUNDS OF SULFURIC ANHYDRIDE

Shustareva, T. K.,Druzhinina, V. E.

, p. 28 - 33 (1986)

By quantitavely studying the sulfonation of thiophene and its homologs by complexes of sulfuric anhydride with ethers, amides and trialkyl phosphates it was possible to determine kinetic and thermodynamic parameters of the process, to propose a SE2 type reaction mechanism and also to reveal a quantitative dependence of the rate constant of the sulfonation reaction of thiophene on the basicity of the complex-forming agent: The sulfonating activity of the complexes studied increses in the series - amides trialkyl phosphates ethers, which is the reverse of the increase in the basicity series of a donor.

Coordination complexes of platinum useful as antiproliferative agents

-

, (2008/06/13)

Platinum complexes are disclosed in which the platinum cation is coordinated to heterocyclic sulfur compounds as well as monodentate or bidentate amines. The complexes have the formula: STR1 wherein L1 and L2 are individually ammonia or monodentate amine ligands or L1 and L2 together are a bidentate amine ligand, S* is sulfur and R1 and R2 taken together with S are thiophene, thiazole, benzothiazole or benzothiophene. These platinum complexes, which have anti-neoplastic activity, are synthesized by reacting sulfonated heterocyclic sulfur compounds with diamines of platinum nitrate.

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