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74537-63-6

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74537-63-6 Usage

Structure

Thiazole derivative with a hydroxyl group attached to the sixth carbon atom of the benzothiazole ring

Usage

Industrial and pharmaceutical applications, building block for the synthesis of other organic compounds, production of dyes, pharmaceuticals, and agricultural chemicals

Potential

Biological activity, potential use in the development of novel drugs

Additional research needed

To fully understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 74537-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,5,3 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 74537-63:
(7*7)+(6*4)+(5*5)+(4*3)+(3*7)+(2*6)+(1*3)=146
146 % 10 = 6
So 74537-63-6 is a valid CAS Registry Number.

74537-63-6SDS

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 6-hydroxy-2-mercapto-benzothiazole

1.2 Other means of identification

Product number -
Other names -

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:74537-63-6 SDS

74537-63-6Upstream product

74537-63-6Relevant articles and documents

Homogeneous photodegradation study of 2-mercaptobenzothiazole photocatalysed by sodium decatungstate salts: Kinetics and mechanistic pathways

Allaoui,Malouki,Wong-Wah-Chung

experimental part, p. 153 - 160 (2010/11/17)

The photochemical degradation of a benzothiazole derivative, 2-mercaptobenzothiazole (MBT) has been studied in aqueous solution in the presence of a polyoxometalate (POM): sodium decatungstate salts Na4W10O32 (DTA). In aerated conditions, the photodegradation rate of MBT clearly increased in the presence of DTA by a factor six when compared with the direct photolysis with kMBT = 0.25 h-1 and t1/2(MBT) = 2.8 h. For the total comprehension of the degradation mechanism, the oxygen influence has been investigated. Oxygen appeared essential for DTA regeneration, its absence induced a three times inhibition of MBT disappearance and completely stopped the photocatalytic cycle. The main photoproducts were identified with LC-ESI-MS and LC-DAD techniques and using some calculations obtained by B3LYP/6-21G method in Gaussian 4.1 software. All the results allowed to propose a mechanistic pathway. Electron transfer and H atom abstraction processes involving W10O324-* excited state species were involved in the degradation. In the primary step of the degradation, the hydroxylation of the aromatic ring leading to four OH-MBT isomers and the formation of disulfide form of MBT were observed. For longer irradiation time, a secondary electron transfer permitted the oxidation of OH-MBT isomers and the formation of sulfoxide derivatives. For prolonged exposure (around 100 h), the complete mineralization was noticed in the presence of sodium decatungstate salts.

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