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91715-47-8

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91715-47-8 Usage

Description

Benzo[b]thiophene, 5,6-dimethoxyis a heterocyclic chemical compound with the molecular formula C11H10O2S. It belongs to the class of organic compounds known as benzene and substituted derivatives. Benzo[b]thiophene, 5,6-dimethoxyfeatures a ring structure containing at least one atom other than carbon, which in this case is sulfur. Benzo[b]thiophene, 5,6-dimethoxyis commonly used in the fields of chemistry and pharmaceuticals, and has been studied for its potential applications in the development of new drugs and materials. Additionally, it has been identified as a component of certain natural products and has been investigated for its biological activities and potential industrial uses.

Uses

Used in Pharmaceutical Industry:
Benzo[b]thiophene, 5,6-dimethoxyis used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
Benzo[b]thiophene, 5,6-dimethoxyis used as a research tool in the field of organic chemistry to study the properties and reactions of heterocyclic compounds. It can provide insights into the synthesis and modification of related compounds for various applications.
Used in Material Science:
Benzo[b]thiophene, 5,6-dimethoxyis used in the development of new materials with specific properties, such as electronic, optical, or mechanical characteristics. Its unique structure and functional groups can contribute to the creation of advanced materials for various industries.
Used in Natural Product Analysis:
As a component of certain natural products, Benzo[b]thiophene, 5,6-dimethoxyis used in the analysis and identification of bioactive compounds found in plants, fungi, and other organisms. This can lead to the discovery of new bioactive compounds with potential applications in medicine, agriculture, and other fields.
Used in Industrial Applications:
Benzo[b]thiophene, 5,6-dimethoxyhas been investigated for its potential industrial uses, such as in the development of new chemical processes or as a component in the production of various industrial products. Its unique properties and reactivity may offer advantages in specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 91715-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,1 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91715-47:
(7*9)+(6*1)+(5*7)+(4*1)+(3*5)+(2*4)+(1*7)=138
138 % 10 = 8
So 91715-47-8 is a valid CAS Registry Number.

91715-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dimethoxy-1-benzothiophene

1.2 Other means of identification

Product number -
Other names 5,6-dimetoxy-1-benzothiophene

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:91715-47-8 SDS

91715-47-8Relevant articles and documents

Mo-Based Oxidizers as Powerful Tools for the Synthesis of Thia- and Selenaheterocycles

Franzmann, Peter,Beil, Sebastian B.,Schollmeyer, Dieter,Waldvogel, Siegfried R.

, p. 1936 - 1940 (2019/01/14)

A highly efficient synthetic protocol for the synthesis of thia- and selenaheterocycles has been developed. By employing a MoCl5-mediated intramolecular dehydrogenative coupling reaction, a broad variety of structural motifs was isolated in yields up to 94 %. The electrophilic key transformation is tolerated by several labile moieties like halides and tertiary alkyl groups. Due to the use of disulfide or diselenide precursors, a high atom efficiency was achieved.

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