5-Bromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine

97%

Reagent Code: #131597
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CAS Number 2064225-89-2

science Other reagents with same CAS 2064225-89-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.96 g/mol
Formula C₁₂H₁₄BBrF₃NO₂
badge Registry Numbers
MDL Number MFCD21365103
thermostat Physical Properties
Boiling Point 349.2±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.45±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily as a building block in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. The presence of bromine and trifluoromethyl groups allows for further functionalization and enhances the electronic properties of the target molecules. It is especially useful in the development of bioactive compounds where the trifluoromethylpyridine motif is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,900.00
inventory 250mg
10-20 days ฿4,990.00
inventory 1g
10-20 days ฿13,300.00

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5-Bromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-(trifluoromethyl)pyridine
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Used primarily as a building block in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. The presence of bromine and trifluoromethyl groups allows for further functionalization and enhances the electronic properties of the target molecules. It is especially useful in the development of bioactive compounds where the trifluoromethylpyridine motif is required.
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