4-Fluorophenylboronic acid
98%
Reagent
Code: #90611
Alias
4-fluorophenylboronic acid; p-fluorophenylboronic acid
CAS Number
1765-93-1
blur_circular Chemical Specifications
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Molecular Information
Weight
139.92 g/mol
Formula
C₆H₆BFO₂
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Registry Numbers
MDL Number
MFCD00039136
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Physical Properties
Melting Point
262-265 °C(lit.)
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Storage & Handling
Storage
2~8°C
description Product Description
4-Fluorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its fluorophenyl group enhances the stability and reactivity of the boronic acid, making it a preferred choice in various catalytic processes. Additionally, it is utilized in the development of sensors and diagnostic reagents due to its ability to interact selectively with specific biological targets.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity (HPLC) | 97.5-100% |
Appearance | White to light yellow powder |
Infrared Spectrum | Conforms to Structure |
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4-Fluorophenylboronic acid
4-Fluorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its fluorophenyl group enhances the stability and reactivity of the boronic acid, making it a preferred choice in various catalytic processes. Additionally, it is utilized in the development of sensors and diagnostic reagents due to its ability to interact selectively with specific biological targets.
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