1-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine

97%

Reagent Code: #242702
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CAS Number 852227-97-5

science Other reagents with same CAS 852227-97-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.20 g/mol
Formula C₁₇H₂₆BNO₂
badge Registry Numbers
MDL Number MFCD07368528
thermostat Physical Properties
Melting Point 156 °C
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The piperidine moiety contributes to enhanced solubility and biological activity in final compounds, often found in active pharmaceutical ingredients (APIs) targeting central nervous system disorders and other therapeutic areas.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,220.00
inventory 1g
10-20 days ฿3,290.00
inventory 5g
10-20 days ฿14,300.00

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1-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The piperidine moiety contributes to enhanced solubility and biological activity in final compounds

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The piperidine moiety contributes to enhanced solubility and biological activity in final compounds, often found in active pharmaceutical ingredients (APIs) targeting central nervous system disorders and other therapeutic areas.

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