N-Ethyl-N-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
97%
Reagent
Code: #219802
CAS Number
2304635-34-3
blur_circular Chemical Specifications
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Molecular Information
Weight
289.19 g/mol
Formula
C₁₆H₂₄BNO₃
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Registry Numbers
MDL Number
MFCD29921699
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Storage & Handling
Storage
2-8°C, dry
description Product Description
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester precursor in the synthesis of complex organic molecules. Its amide functionality provides stability and directs regioselective transformations, making it valuable in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, particularly in the construction of biaryl systems found in active pharmaceutical ingredients. It is also employed in late-stage functionalization due to its compatibility with various functional groups and catalysts.
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