1401577-23-8

Basic information

• Product Name: 2-([1,1':4',1-terphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• CAS NO: 1401577-23-8
• Molecular Weight: 356.272
• Mol File: 1401577-23-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 157 °C
• Boiling Point: 524.1±29.0 °C(Predicted)
• Density: 1.10±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 2-([1,1':4',1-terphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-([1,1':4',1-terphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1401577-23-8)
• EPA Substance Registry System: 2-([1,1':4',1-terphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(1401577-23-8)

Safety Data

• Hazardous Substances Data: 1401577-23-8(Hazardous Substances Data)

Usage

Structure

Dioxaborolane core with boronic ester derivative
The compound has a central 1,3,2-dioxaborolane ring structure, with a boronic ester group attached to a 1-terphenyl group.

Usage in organic synthesis

Suzuki-Miyaura cross-coupling reactions
The compound serves as a reagent in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds.

Applications

Pharmaceutical and agrochemical production
It is used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, contributing to the development of new drugs and chemicals for agriculture.

Potential applications

Medicinal chemistry and materials science
Due to its unique structural and functional properties, the compound has potential for various applications in the fields of medicinal chemistry and materials science, such as the development of new therapeutic agents or advanced materials.

Upstream product

• 144432-80-4 2-(biphenyl-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 92-66-0 4-bromo-1,1'-biphenyl 
• 1762-87-4 3-bromo-p-terphenyl 
• 73183-34-3 bis(pinacol)diborane 
• 1762-86-3 3-chloro-1,1': 4'1-terphenyl 
• 5122-94-1 4-biphenylboronic acid 
• 108-37-2 1-bromo-3-chlorobenzene 

Relevant articles and documents

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