5-TRIFLUOROMETHYLPYRIDINE-2-BORONIC ACID PINACOL ESTER

95%

Reagent Code: #90849
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CAS Number 1101205-23-5

science Other reagents with same CAS 1101205-23-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.06 g/mol
Formula C₁₂H₁₅BF₃NO₂
badge Registry Numbers
MDL Number MFCD07367518
thermostat Physical Properties
Boiling Point 307.3±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.18 g/cm3
Storage -20°C, sealed, dry

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the introduction of the 5-trifluoromethylpyridyl group into various organic molecules, which is valuable in pharmaceutical and agrochemical research. The trifluoromethyl group enhances the biological activity and metabolic stability of the compounds, making it useful in the development of drugs and pesticides. Additionally, its pinacol ester form improves stability and handling, facilitating its use in complex synthetic pathways.

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Test Parameter Specification
Appearance Report Result
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿26,980.00
inventory 10mg
10-20 days ฿12,600.00
inventory 100mg
10-20 days ฿64,800.00

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5-TRIFLUOROMETHYLPYRIDINE-2-BORONIC ACID PINACOL ESTER
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the introduction of the 5-trifluoromethylpyridyl group into various organic molecules, which is valuable in pharmaceutical and agrochemical research. The trifluoromethyl group enhances the biological activity and metabolic stability of the compounds, making it useful in the development of drugs and pesticides. Additionally, its pinacol ester form improves stabili

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the introduction of the 5-trifluoromethylpyridyl group into various organic molecules, which is valuable in pharmaceutical and agrochemical research. The trifluoromethyl group enhances the biological activity and metabolic stability of the compounds, making it useful in the development of drugs and pesticides. Additionally, its pinacol ester form improves stability and handling, facilitating its use in complex synthetic pathways.

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