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Benzothiazole, 2-(dichloromethyl)- (8CI,9CI), also known as 2-(Dichloromethyl)benzothiazole, is an organic compound with the chemical formula C8H5Cl2NS. It is a derivative of benzothiazole, a heterocyclic compound consisting of a benzene ring fused to a thiazole ring. The dichloromethyl group is attached to the 2-position of the benzothiazole ring, making it a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. Benzothiazole, 2-(dichloromethyl)- (8CI,9CI) is known for its versatile reactivity and can be used in various chemical transformations, such as nucleophilic substitutions and electrophilic aromatic substitutions. Due to its potential applications in the synthesis of biologically active compounds, 2-(dichloromethyl)benzothiazole is an important building block in the field of organic chemistry.

6278-69-9

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6278-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6278-69-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6278-69:
(6*6)+(5*2)+(4*7)+(3*8)+(2*6)+(1*9)=119
119 % 10 = 9
So 6278-69-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H5Cl2NS/c9-7(10)8-11-5-3-1-2-4-6(5)12-8/h1-4,7H

6278-69-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dichloromethyl)-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names Benzothiazole, 2-(dichloromethyl)-

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:6278-69-9 SDS

6278-69-9Downstream Products

6278-69-9Relevant academic research and scientific papers

Synthesis of ethenylbenzothiazole derivatives

Ohba,Kosaka,Wakabayashi

, p. 3421 - 3426 (2007/10/03)

Ethenylbenzothiazoles were synthesized by the Horner-Emmons reaction of benzothiazolylmethylphosphonate with aldehydes under phase transfer catalytic conditions in 60-71% yields. Not only aromatic but also aliphatic aldehydes gave the desired products und

Self-Condensation of Benzothiazolylchloromethyllithiums.

Florio, Saverio,Capriati, Vito,Solimini, Maria Cristina,Troisi, Luigino

, p. 8481 - 8484 (2007/10/02)

Benzothiazolylchloromethyllithium 1c and benzothiazolyldichloromethyllithium 1e, easily available by lithiation of 1b and 1d (or 1f) respectively, undergo a different type of self-condensation reaction giving 5 and 7a respectively.The possibility that 1c and 1e behave as halocarbenoids is discussed.

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