N-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzamide
95%
Reagent
Code: #218315
CAS Number
397843-98-0
science Other reagents with same CAS 397843-98-0
blur_circular Chemical Specifications
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Molecular Information
Weight
323.19 g/mol
Formula
C₁₉H₂₂BNO₃
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Registry Numbers
MDL Number
MFCD22415453
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Storage & Handling
Storage
2-8°C
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 industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of biaryl structures found in active pharmaceutical ingredients. Its amide functionality also allows for further derivatization, enhancing its utility in medicinal chemistry and materials science.
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