1256358-97-0

Basic information

• Product Name: 4-Bromo-1h-indole-2-boronic acid pinacol ester
• Synonyms: 4-Bromo-1h-indole-2-boronic acid pinacol ester;4-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole
• CAS NO: 1256358-97-0
• Molecular Formula: C14H17BBrNO2
• Molecular Weight: 340.02056
• Mol File: 1256358-97-0.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Bromo-1h-indole-2-boronic acid pinacol ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-1h-indole-2-boronic acid pinacol ester(1256358-97-0)
• EPA Substance Registry System: 4-Bromo-1h-indole-2-boronic acid pinacol ester(1256358-97-0)

Safety Data

• Hazardous Substances Data: 1256358-97-0(Hazardous Substances Data)

Usage

General Description

4-Bromo-1h-indole-2-boronic acid pinacol ester is a chemical compound used in organic synthesis and drug development. It is a boronic ester derivative of 4-bromo-1h-indole-2-boronic acid, a compound commonly used in Suzuki-Miyaura cross-coupling reactions. This particular ester form is often utilized as a building block for various pharmaceutical and agrochemical compounds due to its reactivity and ability to form carbon-carbon bonds. It is known for its versatility in creating complex organic molecules and serving as a valuable intermediate in the synthesis of biologically active compounds. Additionally, the presence of a bromine group in the compound makes it useful for further derivatization and functionalization in a variety of chemical reactions.