1609267-51-7

Basic information

• Product Name: (9-([1,1':3',1''-terphenyl]-5'-yl)-9H-carbazol-3-yl)boronic acid
• Synonyms: (9-([1,1':3',1''-terphenyl]-5'-yl)-9H-carbazol-3-yl)boronic acid;B-(9-[1,1':3',1''-Terphenyl]-5'-yl-9H-carbazol-3-yl)boronic acid
• CAS NO: 1609267-51-7
• Molecular Formula: C30H22BNO2
• Molecular Weight: 439.31218
• Mol File: 1609267-51-7.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (9-([1,1':3',1''-terphenyl]-5'-yl)-9H-carbazol-3-yl)boronic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (9-([1,1':3',1''-terphenyl]-5'-yl)-9H-carbazol-3-yl)boronic acid(1609267-51-7)
• EPA Substance Registry System: (9-([1,1':3',1''-terphenyl]-5'-yl)-9H-carbazol-3-yl)boronic acid(1609267-51-7)

Safety Data

• Hazardous Substances Data: 1609267-51-7(Hazardous Substances Data)

Usage

General Description

(9-([1,1':3',1''-terphenyl]-5'-yl)-9H-carbazol-3-yl)boronic acid, also known as 9-[5-(3',3''-terphenyl)-9H-carbazol-3-yl]boronic acid, is a boronic acid derivative. It contains a boronic acid functional group attached to a carbazole molecule, which is in turn attached to a terphenyl group. Boronic acids are known for their ability to form reversible covalent bonds with diols and other nucleophiles, making them useful in various organic and medicinal chemistry applications. The specific structure of this compound may give it unique properties or functions within the context of its specific use case, such as in the development of organic electronic materials or as a ligand in metal-catalyzed reactions. The compound's characteristics and potential uses make it of interest to researchers and industry professionals in the fields of chemistry, materials science, and medicinal chemistry.