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33682-62-1

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33682-62-1 Usage

General Description

2(3H)-Benzothiazolethione, 3,6-dimethyl-(9CI) is a chemical compound with the molecular formula C9H9NS. It is a heterocyclic organic compound that contains both sulfur and nitrogen in its ring structure. 2(3H)-Benzothiazolethione,3,6-dimethyl-(9CI) is also known by its other name, 4-methyl-5-phenyl-4,5-dihydro-3H-1,3,4-thiadiazole-2-thione. It has various industrial uses, including as a component in the production of pharmaceuticals, agrochemicals, and dyes. 2(3H)-Benzothiazolethione,3,6-dimethyl-(9CI) also has potential applications in the field of materials science and as a reagent in organic synthesis. Additionally, it possesses interesting biological activities, which make it a potential candidate for drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 33682-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,8 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33682-62:
(7*3)+(6*3)+(5*6)+(4*8)+(3*2)+(2*6)+(1*2)=121
121 % 10 = 1
So 33682-62-1 is a valid CAS Registry Number.

33682-62-1SDS

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 3,6-Dimethyl-1,3-benzothiazole-2(3H)-thione

1.2 Other means of identification

Product number -
Other names 3,6-Dimethyl-3H-benzothiazol-2-on-imin

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:33682-62-1 SDS

33682-62-1Relevant articles and documents

A catalyst-free and additive-free method for the synthesis of benzothiazolethiones from: O -iodoanilines, DMSO and potassium sulfide

Zhu, Xiaoming,Li, Wenguang,Luo, Xiai,Deng, Guobo,Liang, Yun,Liu, Jianbing

, p. 1970 - 1974 (2018/05/23)

Under catalyst-free and additive-free conditions, a novel, convenient, eco-friendly method for the synthesis of benzothiazolethiones has been developed. The three-component reaction of o-iodoanilines and K2S with DMSO proceeded smoothly and the corresponding benzothiazolethiones were obtained with good isolated yields. Meanwhile, this method could be used for the synthesis of thioureas from primary diamines. Furthermore, mechanism research showed that DMSO not only functioned as a carbon source, but also as a mild oxidant in this reaction.

A convenient metal-free method for the synthesis of benzothiazolethiones from o-haloanilines and carbon disulfide

Wang, Fei,Xi, Chanjuan,Zhao, Peng

, p. 1477 - 1480 (2020/01/03)

A convenient method has been developed for the preparation of a variety of 1,3-benzothiazole-2(3H)-thiones. The reaction proceeds from an o-haloaniline derivative and carbon disulfide in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene at 80-140 °C to g

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