1000160-75-7

Basic information

• Product Name: Benzo[b]thiophen-4-ylboronic acid pinacol ester
• Synonyms: Benzo[b]thiophen-4-ylboronic acid pinacol ester;Benzothiophene-4-boronic acid pinacol ester;Benzo[b]thiophene, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-;4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[b]thiophene;2-(benzo[b]thiophen-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• CAS NO: 1000160-75-7
• Molecular Formula: C14H17BO2S
• Molecular Weight: 278
• Product Categories: Benzothiophene;Organoborons
• Mol File: 1000160-75-7.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzo[b]thiophen-4-ylboronic acid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzo[b]thiophen-4-ylboronic acid pinacol ester(1000160-75-7)
• EPA Substance Registry System: Benzo[b]thiophen-4-ylboronic acid pinacol ester(1000160-75-7)

Safety Data

• Hazardous Substances Data: 1000160-75-7(Hazardous Substances Data)

Usage

General Description

Benzo[b]thiophen-4-ylboronic acid pinacol ester is a chemical compound used as a building block in the synthesis of various organic compounds. It consists of a boronic acid functional group attached to a benzo[b]thiophene ring. The pinacol ester group present in the compound provides stability and solubility, making it a useful reagent for Suzuki-Miyaura cross-coupling reactions to form C-C bonds. Benzo[b]thiophen-4-ylboronic acid pinacol ester has applications in the pharmaceutical and agrochemical industries, as well as in materials science for the synthesis of organic semiconductors and polymers. Its unique structure and reactivity make it a valuable tool for chemists in the development of new compounds and materials.