3-Fluoro-5-(trifluoromethyl)phenylboronic acid

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Reagent Code: #90175
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Alias 3-Fluoro-5-trifluoromethylphenylboronic acid
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CAS Number 159020-59-4

science Other reagents with same CAS 159020-59-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.92 g/mol
Formula C₇H₅BF₄O₂
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for introducing fluorinated aromatic groups into complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. The fluorine atoms enhance the metabolic stability and bioavailability of the resulting compounds, making it a preferred choice in drug design. Additionally, it is employed in materials science for creating advanced polymers and electronic materials with specific properties. Its ability to form stable boronate esters also makes it useful in bioconjugation and chemical sensing applications.

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Test Parameter Specification
Purity (HPLC) 97-100
Melting Point (C) 178-180
Purity 97-100
Appearance White to Off-White Powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿400.00
inventory 1g
10-20 days ฿880.00
inventory 5g
10-20 days ฿3,450.00
inventory 25g
10-20 days ฿16,900.00

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3-Fluoro-5-(trifluoromethyl)phenylboronic acid
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This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for introducing fluorinated aromatic groups into complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. The fluorine atoms enhance the metabolic stability and bioavailability of the resulting compounds, making it a preferred choice in drug design. Additionally, it is employed in materials science for creating advanced polymers and electronic materials with specific properties. Its ability to form stable boronate esters also makes it useful in bioconjugation and chemical sensing applications.
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