675571-82-1

Basic information

• Product Name: [1,1'-Biphenyl]-4-amine, N,N-diphenyl-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
• Synonyms: N,N-diphenyl-4′-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,1'-biphenyl]-4-amine
• CAS NO: 675571-82-1
• Molecular Formula: C30H30BNO2
• Molecular Weight: 447.385
• Mol File: 675571-82-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: [1,1'-Biphenyl]-4-amine, N,N-diphenyl-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: [1,1'-Biphenyl]-4-amine, N,N-diphenyl-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-(675571-82-1)
• EPA Substance Registry System: [1,1'-Biphenyl]-4-amine, N,N-diphenyl-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-(675571-82-1)

Safety Data

• Hazardous Substances Data: 675571-82-1(Hazardous Substances Data)

Usage

General Description

The chemical compound "[1,1'-Biphenyl]-4-amine, N,N-diphenyl-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-" is a derivative of biphenyl-4-amine with a boron-containing group attached to one of the phenyl rings. It is commonly used in organic synthesis as a reagent for the Suzuki-Miyaura cross-coupling reaction, which is a widely used method for forming carbon-carbon bonds. [1,1'-Biphenyl]-4-amine, N,N-diphenyl-4'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- is also known for its ability to participate in various other chemical reactions, such as palladium-catalyzed coupling reactions and metal-catalyzed cyanation reactions. It is a valuable tool for the construction of complex organic molecules and has applications in pharmaceutical, agrochemical, and material science research.

Upstream product

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Downstream Products

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