3-Formylphenylboronic acid

≥98%

Reagent Code: #90258
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Alias 3-Formylphenylboronic acid
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CAS Number 87199-16-4

science Other reagents with same CAS 87199-16-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.94 g/mol
Formula C₇H₇BO₃
badge Registry Numbers
MDL Number MFCD00161356
thermostat Physical Properties
Melting Point 182-186 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for creating biaryl structures. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it serves as a building block in the synthesis of complex organic molecules, including polymers and materials with specific electronic properties. The formyl group further allows for functionalization, making it versatile in designing compounds for applications in catalysis, sensors, and advanced materials. Its role in medicinal chemistry is notable, as it aids in the development of targeted therapies and bioactive molecules.

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Test Parameter Specification
Purity (HPLC) 98-100
Melting Point (°C) 109-113

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿280.00
inventory 5g
10-20 days ฿590.00
inventory 25g
10-20 days ฿2,500.00
inventory 100g
10-20 days ฿9,790.00

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3-Formylphenylboronic acid
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for creating biaryl structures. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it serves as a building block in the synthesis of complex organic molecules, including polymers and materials with specific electronic properties. The formyl group further allows for functionalization, making it versatile in designing compounds for applications in catalysis, sensors, and advanced materials. Its role in medicinal chemistry is notable, as it aids in the development of targeted therapies and bioactive molecules.
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