6-Bromopyridine-3-boronic acid

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Reagent Code: #90962
label
Alias 6-Bromopyridine-3-boronic acid
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CAS Number 223463-14-7

science Other reagents with same CAS 223463-14-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.82 g/mol
Formula C₅H₅BBrNO₂
badge Registry Numbers
MDL Number MFCD03411558
thermostat Physical Properties
Melting Point 161-166 °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 complex biaryl compounds in pharmaceutical research. It plays a role in creating drug candidates, particularly in the development of kinase inhibitors for cancer treatment. Also employed in material science for constructing organic electronic materials and polymers. Its boronic acid group allows for selective binding in sensor applications, aiding in the detection of biological molecules.

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Test Parameter Specification
Purity (HPLC) 97.5-100
Melting Point 155-165
Appearance White to tan powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿15,280.00
inventory 1g
10-20 days ฿480.00
inventory 5g
10-20 days ฿1,180.00
inventory 25g
10-20 days ฿4,630.00

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6-Bromopyridine-3-boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical research. It plays a role in creating drug candidates, particularly in the development of kinase inhibitors for cancer treatment. Also employed in material science for constructing organic electronic materials and polymers. Its boronic acid group allows for selective binding in sensor applications, aiding in the detection of biological molecules.

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical research. It plays a role in creating drug candidates, particularly in the development of kinase inhibitors for cancer treatment. Also employed in material science for constructing organic electronic materials and polymers. Its boronic acid group allows for selective binding in sensor applications, aiding in the detection of biological molecules.

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