4-Bromomethylphenylboronic acid pinacol ester

95%

Reagent Code: #90662
label
Alias 2-(4-Bromomethylphenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborinane 4-Bromomethylphenylboronic acid pinadate
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CAS Number 138500-85-3

science Other reagents with same CAS 138500-85-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297 g/mol
Formula C₁₃H₁₈BBrO₂
badge Registry Numbers
MDL Number MFCD02179493
thermostat Physical Properties
Melting Point 83-85°C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds widely applied in pharmaceuticals and organic materials.

Acts as a building block in the preparation of boron-containing molecules, which are essential in drug discovery and development.

Employed in the modification of organic frameworks, enhancing properties for use in sensors and optoelectronic devices.

Facilitates the creation of complex molecular structures in medicinal chemistry, particularly in the design of enzyme inhibitors and receptor ligands.

Applied in the development of advanced materials, including polymers and liquid crystals, for industrial and research purposes.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 83-89
Purity (GC) 95-100
Purity (Titration with AgNO3) 94.5-105.5
Appearance White to tan powder, crystals and/or chunks
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿520.00
inventory 5g
10-20 days ฿1,790.00
inventory 25g
10-20 days ฿7,550.00

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4-Bromomethylphenylboronic acid pinacol ester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds widely applied in pharmaceuticals and organic materials.

Acts as a building block in the preparation of boron-containing molecules, which are essential in drug discovery and development.

Employed in the modification of organic frameworks, enhancing properties for use in sensors and optoelectronic devices.

Facilitates the creation of complex molecular structures in medicinal

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of biaryl compounds widely applied in pharmaceuticals and organic materials.

Acts as a building block in the preparation of boron-containing molecules, which are essential in drug discovery and development.

Employed in the modification of organic frameworks, enhancing properties for use in sensors and optoelectronic devices.

Facilitates the creation of complex molecular structures in medicinal chemistry, particularly in the design of enzyme inhibitors and receptor ligands.

Applied in the development of advanced materials, including polymers and liquid crystals, for industrial and research purposes.

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