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24097-02-7

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24097-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24097-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,9 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24097-02:
(7*2)+(6*4)+(5*0)+(4*9)+(3*7)+(2*0)+(1*2)=97
97 % 10 = 7
So 24097-02-7 is a valid CAS Registry Number.

24097-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenylbenzo[d]thiazole-2(3H)-thione

1.2 Other means of identification

Product number -
Other names 3-Phenyl-2-benzothiazolthion.

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:24097-02-7 SDS

24097-02-7Downstream Products

24097-02-7Relevant articles and documents

Cleaner and greener synthesis of 3H-benzothiazole-2-thione and its derivatives

Srivastava, Nitin,Kishore, Ram

, p. 29 - 39 (2020/08/14)

A cleaner and greener method of synthesis of 3H-benzothiazole-2-thione is being reported in this communication. In this method, various o-iodoaniline derivatives are reacted with carbon disulfide in the presence of Cs2CO3 and tetramethyl ammonium bromide (TMAB) to give 3H-benzothiazole-2-thione and its derivatives in higher yields.

Copper-Catalyzed Three-Component Synthesis of Benzothiazolethiones from o-Iodoanilines, Isocyanide, and Potassium Sulfide

Dang, Pan,Zeng, Weilan,Liang, Yun

, p. 34 - 37 (2015/07/28)

An efficient copper catalyzed strategy for the synthesis of a variety of benzothiazolethione derivatives has been developed. In the presence of CuCl, the three-component reaction of o-iodoanilines and K2S with p-toluenesulfonylmethyl isocyanide proceeded smoothly to obtain the corresponding benzothiazolethiones in good to excellent isolated yields. Notably, isocyanide functioned as a carbon source and K2S functioned as a sulfur source in this reaction.

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