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6-Chlorobenzo[b]thiophene is a chlorinated derivative of benzo[b]thiophene, a heterocyclic aromatic compound with a molecular formula of C8H5ClS. It features a thiophene ring fused to a benzene ring, and the presence of the chlorine atom in its molecular structure imparts unique chemical properties, making it a significant intermediate in the synthesis of various organic compounds.

66490-20-8

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66490-20-8 Usage

Uses

Used in Pharmaceutical Industry:
6-Chlorobenzo[b]thiophene is used as a building block for the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 6-chlorobenzo[b]thiophene serves as a key intermediate in the production of various agrochemicals, aiding in the creation of effective pest control and crop protection solutions.
Used in Organic Electronics:
6-Chlorobenzo[b]thiophene is utilized in the synthesis of organic electronic materials, playing a crucial role in the advancement of organic semiconductors and other electronic components.
Used in Optoelectronic Applications:
It has been studied for its potential use in the development of new materials for optoelectronic applications, where its unique properties can contribute to the performance of devices such as solar cells and light-emitting diodes (LEDs).

Check Digit Verification of cas no

The CAS Registry Mumber 66490-20-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,9 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66490-20:
(7*6)+(6*6)+(5*4)+(4*9)+(3*0)+(2*2)+(1*0)=138
138 % 10 = 8
So 66490-20-8 is a valid CAS Registry Number.

66490-20-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chloro-1-benzothiophene

1.2 Other means of identification

Product number -
Other names Benzo[b]thiophene,6-chloro

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:66490-20-8 SDS

66490-20-8Downstream Products

66490-20-8Relevant academic research and scientific papers

(AZA)INDOLE-, BENZOTHIOPHENE-, AND BENZOFURAN-3-SULFONAMIDES

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, (2018/07/29)

Disclosed are sulfonamide compounds with GPR17 modulating properties, which are useful for treating or preventing a variety of CNS and other diseases, in particular for preventing and treating myelinating diseases or disorders.

GLUCOSYLCERAMIDE SYNTHASE INHIBITORS FOR THE TREATMENT OF DISEASES

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, (2015/04/15)

Described herein are compounds of Formula I, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or conditions associated with the enzyme glucosylceramide synthase (GCS).

An improved synthesis of substituted benzo[b]thiophenes using microwave irradiation

Allen, Daniel,Callaghan, Owen,Cordier, Frederic L.,Dobson, David R.,Harris, John R.,Hotten, Terry M.,Owton, W. Martin,Rathmell, Richard E.,Wood, Virginia A.

, p. 9645 - 9647 (2007/10/03)

An easy and high-yielding method for the synthesis of substituted benzo[b]thiophenes using microwave irradiation is described.

Indole derivatives for the treatment of depression and anxiety

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Page/Page column 38, (2010/02/05)

The present invention provides compounds of formula (I): which are useful for treating depression, anxiety, and alleviating the symptoms caused by withdrawal or partial withdrawal from the use of tobacco or of nicotine.

Substituted oxoazaheterocyclyl compounds

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Page/Page column 68, (2008/06/13)

This invention is directed to oxoazaheterocycyl compounds which inhibit Factor Xa, to oxoazaheterocycyl compounds which inhibit both Factor Xa and Factor IIa, to pharmaceutical compositions comprising these compounds, to intermediates useful for preparing these compounds, to a method of directly inhibiting Factor Xa and to a method of simultaneously directly inhibiting Factor Xa and Factor IIa..

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