N-Allyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
98%
Reagent
Code: #215674
CAS Number
2251118-07-5
blur_circular Chemical Specifications
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Molecular Information
Weight
287.16 g/mol
Formula
C₁₆H₂₂BNO₃
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Registry Numbers
MDL Number
MFCD28347971
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Physical Properties
Boiling Point
429.9±38.0 °C(Predicted)
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Storage & Handling
Density
1.06±0.1 g/cm3(Predicted)
Storage
2-8°C, Sealed, Inert Gas
description Product Description
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical and agrochemical research. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. The allylamide moiety allows further functionalization, making it valuable in the development of bioactive molecules and organic materials. Commonly employed in medicinal chemistry for constructing drug-like scaffolds and in the preparation of boron-containing compounds for imaging or therapeutic applications.
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