N-(Prop-2-yn-1-yl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
95%
Reagent
Code: #219636
CAS Number
1357387-28-0
blur_circular Chemical Specifications
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Molecular Information
Weight
285.15 g/mol
Formula
C₁₆H₂₀BNO₃
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Registry Numbers
MDL Number
MFCD20275029
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Physical Properties
Melting Point
90-95 °C
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Storage & Handling
Storage
2-8°C, Inert Gas
description Product Description
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl and heterobiaryl systems. Its alkyne-functionalized amide moiety allows further modification via click chemistry, enabling rapid diversification in drug discovery and materials science. Due to its dual functionality, it is widely employed in the development of bioactive compounds and functional polymers.
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