2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
95%
Reagent
Code: #206637
CAS Number
660867-80-1
blur_circular Chemical Specifications
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Molecular Information
Weight
219.09 g/mol
Formula
C₁₂H₁₈BNO₂
thermostat
Physical Properties
Melting Point
66-71°C
Boiling Point
315.9°C
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Storage & Handling
Storage
2-8°C
description Product Description
Used primarily in cross-coupling reactions, this compound serves as a key reagent in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in constructing biaryl and heteroaryl frameworks found in active pharmaceutical ingredients. The pyridine ring enhances solubility and coordination properties, improving reaction efficiency in palladium-catalyzed processes. Commonly employed in late-stage functionalization, it supports the rapid diversification of molecular structures in drug discovery and materials science.
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2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Used primarily in cross-coupling reactions, this compound serves as a key reagent in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in constructing biaryl and heteroaryl frameworks found in active pharmaceutical ingredients. The pyridine ring enhances solubility and coordination properties, improving reaction efficiency in palladium-catalyzed processes. Commonly employed in late-stage functionalization, it supports the rapid diversification of molecular structures in drug discovery and materials science.
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