N-Phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
97%
Reagent
Code: #215907
CAS Number
1395316-08-1
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
MFCD24039903
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Physical Properties
Boiling Point
408.1±28.0 °C(Predicted)
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Storage & Handling
Density
1.13±0.1 g/cm3(Predicted)
Storage
2-8°C, sealed, dry
description Product Description
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of organic electronic materials and conjugated polymers due to its stability and reactivity profile. Also utilized in medicinal chemistry for constructing complex aromatic amide structures with potential biological activity.
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