374933-76-3

Basic information

• Product Name: (6-BroMobenzo[b]thiophen-2-yl)Methanol
• Synonyms: (6-BroMobenzo[b]thiophen-2-yl)Methanol
• CAS NO: 374933-76-3
• Molecular Formula: C₉H₇BrOS
• Molecular Weight: 243.12028
• Mol File: 374933-76-3.mol
• Article Data: 9

Chemical Properties

• Melting Point: 107～109℃
• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (6-BroMobenzo[b]thiophen-2-yl)Methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (6-BroMobenzo[b]thiophen-2-yl)Methanol(374933-76-3)
• EPA Substance Registry System: (6-BroMobenzo[b]thiophen-2-yl)Methanol(374933-76-3)

Safety Data

• Hazardous Substances Data: 374933-76-3(Hazardous Substances Data)

Usage

General Description

(6-Bromobenzo[b]thiophen-2-yl)methanol is a chemical compound with the molecular formula C9H7BrOS. It is a derivative of benzo[b]thiophene, which is a bicyclic aromatic compound containing a thiophene ring fused to a benzene ring. The presence of a bromine atom in the molecule gives it unique chemical properties and reactivity. (6-BroMobenzo[b]thiophen-2-yl)Methanol has potential applications in organic synthesis and pharmaceutical research due to its structural features. It may be used as a building block for the synthesis of other organic compounds or as a starting material for the development of new drugs. Additionally, it may have potential use in materials science due to its aromatic nature and potential electronic properties. Overall, (6-bromobenzo[b]thiophen-2-yl)methanol is a versatile chemical compound with a range of potential applications in various fields of chemistry and materials science.

Upstream product

• 2365-48-2 Methyl thioglycolate 
• 57848-46-1 4-bromo-2-fluorobenzaldehyde 
• 5629-98-1 2,4-dibromobenzaldehyde 
• 360576-01-8 6-bromo-benzo[b]thiophene-2-carboxylic acid methyl ester 
• 105191-64-8 6-Brombenzothiophen-2-carbonsaeure-ethylester 
• 105191-52-4 5-(2,4-Dibrombenzyliden)-2-thioxothiazolidin-4-on 
• 105212-27-9 6-Brombenzothiophen-2-carbonylchlorid 
• 19075-58-2 6-bromo-1-benzothiophene-2-carboxylic acid 

Downstream Products

• 912332-92-4 6-bromo-2-methylbenzo[b]thiophene 
• 1133006-91-3 N-(4-methoxybenzyl)-N-((6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[b]thiophen-2-yl)methyl)methanesulfonamide 
• 1132970-31-0 N-((6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)benzo[b]thiophen-2-yl)methyl)methanesulfonamide 
• 1190198-24-3 6-bromo-1-benzothiophene-2-carbonitrile 
• 895550-11-5 6-bromo-2-(bromomethyl)benzo[b]thiophene 
• 19075-45-7 6-bromobenzo[b]thiophene-2-carbaldehyde 

Relevant articles and documents

Benzothiophene-flanked diketopyrrolopyrrole polymers: Impact of isomeric frameworks on carrier mobilities

Exploring new building blocks for solution-processable polymeric semiconductors has attracted much attention. We herein develop two isomeric benzothiophene-flanked diketopyrrolopyrrole polymers with different linkage positions and further systematically study the electronic structures, optical properties, and field-effect characteristics. Both polymers exhibit typical p-type transport characteristics with the highest mobility being up to 0.80 cm2 V-1 s-1. Our results suggest that the isomeric backbones for conjugated polymers greatly affect charge transport properties.

Radioactive iodine labeled compound, and, radioactive pharmaceutical containing the same (by machine translation)

PROBLEM TO BE SOLVED: and compatibility and affinity for both amyloidosis acryloyldimethyltauric, labeled compd. radioactive iodine. SOLUTION: the present invention, N, N-labeled compd. dimethyl benzene amine including radioactive iodine or its salt. Selected drawing: no (by machine translation)

Synthesis of a ferrocene-functionalized unsymmetrical benzo[b]thienyl- thienylethene photoswitch with a cyclopentene core

A new and potentially general synthetic route toward unsymmetrical benzo[b]thienyl-thienylethene compounds is described, with specific focus on conjugation of a ferrocene to the benzo[b]thiophene subunit. The route proceeds in an overall yield of 17%. Copyright