(6-(Trifluoromethoxy)pyridin-3-yl)boronic acid

97%

Reagent Code: #90937
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CAS Number 1008140-70-2

science Other reagents with same CAS 1008140-70-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.92 g/mol
Formula C₆H₅BF₃NO₃
badge Registry Numbers
MDL Number MFCD07374890
thermostat Physical Properties
Boiling Point 259.7±50.0°C
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 intermediate for the construction of complex molecules, especially in the pharmaceutical and agrochemical industries. Its trifluoromethoxy group enhances the biological activity and metabolic stability of the resulting compounds, making it valuable in drug discovery. Additionally, it is employed in the development of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to modify electronic properties. Its boronic acid functionality allows for efficient conjugation with various organic substrates, facilitating the creation of diverse chemical structures.

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Test Parameter Specification
Appearance White to Off-white Solid
Purity (%) 96.5-100
Mass Spectrum Conforms to Structure
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿6,849.00

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(6-(Trifluoromethoxy)pyridin-3-yl)boronic 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 intermediate for the construction of complex molecules, especially in the pharmaceutical and agrochemical industries. Its trifluoromethoxy group enhances the biological activity and metabolic stability of the resulting compounds, making it valuable in drug discovery. Additionally, it is employed in the development of advanced materials, such as organic semiconductors and l

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex molecules, especially in the pharmaceutical and agrochemical industries. Its trifluoromethoxy group enhances the biological activity and metabolic stability of the resulting compounds, making it valuable in drug discovery. Additionally, it is employed in the development of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to modify electronic properties. Its boronic acid functionality allows for efficient conjugation with various organic substrates, facilitating the creation of diverse chemical structures.

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