4-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER

98%

Reagent Code: #90521
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CAS Number 214360-65-3

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.07 g/mol
Formula C₁₃H₁₆BF₃O₂
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is widely used in Suzuki-Miyaura cross-coupling reactions, a pivotal method in organic synthesis for forming carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it suitable for constructing complex organic molecules, particularly in the synthesis of aromatic compounds. Additionally, it is employed in the development of liquid crystals and organic electronic materials, where precise molecular architecture is crucial. Its trifluoromethyl group enhances the lipophilicity and metabolic stability of the final products, making it valuable in drug discovery and development.

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Test Parameter Specification
Purity 98-100%
Appearance White to off-white solid
Proton NMR Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿5,840.00
inventory 200mg
10-20 days ฿280.00
inventory 1g
10-20 days ฿480.00
inventory 5g
10-20 days ฿1,520.00

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4-TRIFLUOROMETHYLPHENYLBORONIC ACID, PINACOL ESTER
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This compound is widely used in Suzuki-Miyaura cross-coupling reactions, a pivotal method in organic synthesis for forming carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it suitable for constructing complex organic molecules, particularly in the synthesis of aromatic compounds. Additionally, it is employed in the development of liquid crystals and organic electronic materials, where precis

This compound is widely used in Suzuki-Miyaura cross-coupling reactions, a pivotal method in organic synthesis for forming carbon-carbon bonds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it suitable for constructing complex organic molecules, particularly in the synthesis of aromatic compounds. Additionally, it is employed in the development of liquid crystals and organic electronic materials, where precise molecular architecture is crucial. Its trifluoromethyl group enhances the lipophilicity and metabolic stability of the final products, making it valuable in drug discovery and development.

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