3-Carboxy-5-fluorobenzeneboronic acid

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Reagent Code: #90273
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CAS Number 871329-84-9

science Other reagents with same CAS 871329-84-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.93 g/mol
Formula C₇H₆BFO₄
badge Registry Numbers
MDL Number MFCD07363791
inventory_2 Storage & Handling
Density 1.49±0.1 g/cm3 (20 ºC 760 Torr)
Storage 2~8°C

description Product Description

Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of various bioactive molecules. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, which are essential for creating complex organic compounds, including potential drug candidates. The fluorine atom enhances its ability to interact with biological targets, making it valuable in the design of fluorinated pharmaceuticals. Additionally, it is utilized in materials science for the preparation of advanced polymers and coatings with specific functional properties.

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Test Parameter Specification
Melting point 264-266
Purity (HPLC) 98-100
Appearance White to yellow powder or crystals
Infrared Spectrum Conforms to Structure
NMR Spectrum Conforms to Structure

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inventory 1g
10-20 days ฿1,840.00

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3-Carboxy-5-fluorobenzeneboronic acid
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Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of various bioactive molecules. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, which are essential for creating complex organic compounds, including potential drug candidates. The fluorine atom enhances its ability to interact with biological targets, making it valuable in the design of fluorinated pharmaceuticals. Additionally, it is

Used primarily in organic synthesis and pharmaceutical research, this compound serves as a key intermediate in the development of various bioactive molecules. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, which are essential for creating complex organic compounds, including potential drug candidates. The fluorine atom enhances its ability to interact with biological targets, making it valuable in the design of fluorinated pharmaceuticals. Additionally, it is utilized in materials science for the preparation of advanced polymers and coatings with specific functional properties.

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