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2,3-dibromo-1-benzothiophene 1,1-dioxide is a heterocyclic chemical compound with the molecular formula C8H4Br2O2S. It features a benzene ring fused to a thieno[3,4-d]thiazine-1,1-dioxide skeleton, with two bromine atoms attached to the benzene ring. This white to light yellow crystalline solid is a versatile building block in organic synthesis and has potential applications across various fields, including pharmaceuticals, agrochemicals, and materials science. Its chemical structure also suggests possible biological activities, making it a candidate of interest in medicinal chemistry research.

19163-38-3

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19163-38-3 Usage

Uses

Used in Pharmaceutical Industry:
2,3-dibromo-1-benzothiophene 1,1-dioxide serves as a key intermediate in the synthesis of pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic effects, making it valuable in medicinal chemistry for creating novel pharmaceutical agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3-dibromo-1-benzothiophene 1,1-dioxide is utilized as a precursor in the production of pesticides and other agrochemicals. Its chemical properties contribute to the creation of effective compounds for crop protection and enhancement of agricultural yields.
Used in Materials Science:
2,3-dibromo-1-benzothiophene 1,1-dioxide is employed as a building block in the synthesis of advanced materials with specific properties. Its incorporation into material compositions can lead to the development of new polymers, composites, or other materials with applications in various industries, such as electronics, textiles, or coatings.
Used in Organic Synthesis:
As a versatile intermediate, 2,3-dibromo-1-benzothiophene 1,1-dioxide is used in various organic synthesis processes. Its reactivity and structural features make it suitable for the preparation of more complex organic compounds, which can be further utilized in different chemical and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 19163-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,6 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19163-38:
(7*1)+(6*9)+(5*1)+(4*6)+(3*3)+(2*3)+(1*8)=113
113 % 10 = 3
So 19163-38-3 is a valid CAS Registry Number.

19163-38-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dibromobenzo[b]-thiophene

1.2 Other means of identification

Product number -
Other names 2,3-dibromobenzo[b]thophene

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:19163-38-3 SDS

19163-38-3Relevant academic research and scientific papers

A novel aggregation-induced emission platform from 2,3-diphenylbenzo[b]thiophene S,S-dioxide

Guo, Jingjing,Hu, Shimin,Luo, Wenwen,Hu, Rongrong,Qin, Anjun,Zhao, Zujin,Tang, Ben Zhong

supporting information, p. 1463 - 1466 (2017/02/05)

New aggregation-induced emission (AIE) luminogens with high solid-state emission efficiencies are developed by adopting a benzo[b]thiophene S,S-dioxide core, and steric and electronic effects on the AIE property are elucidated.

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