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

95%

Reagent Code: #226644
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CAS Number 852228-08-1

science Other reagents with same CAS 852228-08-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.19 g/mol
Formula C₁₆H₂₅BN₂O₂
badge Registry Numbers
MDL Number MFCD06798274
thermostat Physical Properties
Melting Point 110 - 114 ℃
Boiling Point 427.8 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.07±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyridine-based structures in pharmaceuticals and agrochemicals. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of bioactive molecules, particularly in drug discovery programs targeting kinase inhibitors and CNS-active compounds. Also applied in materials science for constructing conjugated systems in organic electronics.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,330.00
inventory 5g
10-20 days ฿4,970.00
inventory 25g
10-20 days ฿24,710.00

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2-(Piperidin-1-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyridine-based structures in pharmaceuticals and agrochemicals. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of bioactive molecules, particularly in drug discovery programs targeting kinase inhibitors and CNS-active compounds. Also applied in materials science for constructing conjugated systems in organic elect

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyridine-based structures in pharmaceuticals and agrochemicals. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of bioactive molecules, particularly in drug discovery programs targeting kinase inhibitors and CNS-active compounds. Also applied in materials science for constructing conjugated systems in organic electronics.

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