N-Isopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
95%
Reagent
Code: #215641
CAS Number
1036990-35-8
blur_circular Chemical Specifications
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Molecular Information
Weight
289.18 g/mol
Formula
C₁₆H₂₄BNO₃
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Registry Numbers
MDL Number
MFCD22493990
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Physical Properties
Boiling Point
423.9±28.0 °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 industries. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl systems. Its amide functionality allows for further derivatization or integration into larger molecular frameworks, enhancing its utility in drug discovery and development. The presence of the isopropyl group can influence solubility and reactivity, offering advantages in reaction optimization and selectivity.
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