N-Methyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)acetamide
≥98%
Reagent
Code: #215879
CAS Number
1421341-01-6
blur_circular Chemical Specifications
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Molecular Information
Weight
289.18 g/mol
Formula
C₁₆H₂₄BNO₃
thermostat
Physical Properties
Boiling Point
418.2±38.0 °C(Predicted)
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Storage & Handling
Density
1.05±0.1 g/cm3(Predicted)
Storage
2-8°C, Sealed, 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 presence of the boronate ester group enables efficient carbon-carbon bond formation under mild palladium-catalyzed conditions. Its amide functionality provides stability and can act as a directing or protecting group during multi-step syntheses. Due to its bifunctional nature, it is valuable in constructing biaryl and heterobiaryl systems found in bioactive compounds and functional materials.
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