(4'-Chloro-[1,1'-biphenyl]-4-yl)boronic acid

98%

Reagent Code: #90294
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CAS Number 364044-44-0

science Other reagents with same CAS 364044-44-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.47 g/mol
Formula C₁₂H₁₀BClO₂
thermostat Physical Properties
Boiling Point 411°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex biphenyl structures. These structures are often found in pharmaceuticals, agrochemicals, and materials science. Its chloro and boronic acid functional groups make it a versatile building block for designing molecules with specific properties, such as enhanced stability or biological activity. Additionally, it is employed in the development of organic electronic materials, where precise molecular architecture is crucial for performance.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity 97.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿710.00
inventory 1g
10-20 days ฿1,750.00
inventory 5g
10-20 days ฿5,430.00
inventory 25g
10-20 days ฿18,410.00

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(4'-Chloro-[1,1'-biphenyl]-4-yl)boronic acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex biphenyl structures. These structures are often found in pharmaceuticals, agrochemicals, and materials science. Its chloro and boronic acid functional groups make it a versatile building block for designing molecules with specific properties, such as enhanced stability or biological act

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the construction of complex biphenyl structures. These structures are often found in pharmaceuticals, agrochemicals, and materials science. Its chloro and boronic acid functional groups make it a versatile building block for designing molecules with specific properties, such as enhanced stability or biological activity. Additionally, it is employed in the development of organic electronic materials, where precise molecular architecture is crucial for performance.

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