3-Fluoro-5-(hydroxymethyl)phenylboronic Acid

≥95%

Reagent Code: #90174
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CAS Number 1146614-40-5

science Other reagents with same CAS 1146614-40-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.95 g/mol
Formula C₇H₈FO₃B
badge Registry Numbers
MDL Number MFCD19687060
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex molecules used in pharmaceuticals and materials science. Its boronic acid group facilitates coupling with aryl halides, while the hydroxymethyl group offers additional functionalization opportunities. The fluorine atom enhances stability and can influence the electronic properties of the resulting products. It is also employed in the development of bioactive compounds, including potential drug candidates, due to its ability to introduce fluorine atoms into target molecules, which can improve metabolic stability and binding affinity. Additionally, it finds use in the synthesis of advanced materials, such as organic semiconductors and polymers.

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Test Parameter Specification
Appearance White to yellow solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,970.00
inventory 1g
10-20 days ฿38,900.00

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3-Fluoro-5-(hydroxymethyl)phenylboronic Acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex molecules used in pharmaceuticals and materials science. Its boronic acid group facilitates coupling with aryl halides, while the hydroxymethyl group offers additional functionalization opportunities. The fluorine atom enhances stability and can influence the electronic properties of the resulting pr

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex molecules used in pharmaceuticals and materials science. Its boronic acid group facilitates coupling with aryl halides, while the hydroxymethyl group offers additional functionalization opportunities. The fluorine atom enhances stability and can influence the electronic properties of the resulting products. It is also employed in the development of bioactive compounds, including potential drug candidates, due to its ability to introduce fluorine atoms into target molecules, which can improve metabolic stability and binding affinity. Additionally, it finds use in the synthesis of advanced materials, such as organic semiconductors and polymers.

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