N,N,3-Trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
96%
Reagent
Code: #215662
CAS Number
2096337-88-9
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
MFCD18434458
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Physical Properties
Boiling Point
439.4±45.0 °C(Predicted)
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Storage & Handling
Density
1.05±0.1 g/cm3(Predicted)
Storage
Room temperature, seal, dry
description Product Description
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its amide functionality provides a handle for further derivatization or integration into biologically active molecules. Commonly employed in the development of pharmaceuticals and agrochemicals where aryl-aryl bond formation is required. The presence of the methyl and amide groups can influence electronic and steric properties, making it useful in fine-tuning reaction outcomes. Also applied in materials science for constructing conjugated systems in organic electronics.
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