N-(2-(Piperidin-1-yl)ethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
≥95%
Reagent
Code: #215576
CAS Number
2828439-61-6
blur_circular Chemical Specifications
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Molecular Information
Weight
358.28 g/mol
Formula
C₂₀H₃₁BN₂O₃
thermostat
Physical Properties
Boiling Point
514.1±35.0 °C(Predicted)
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Storage & Handling
Density
1.09±0.1 g/cm3(Predicted)
Storage
2-8°C, Sealed, Inert Gas
description Product Description
Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds in pharmaceutical development. Its boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Commonly employed in the preparation of bioactive molecules, particularly in drug discovery programs targeting kinase inhibitors and CNS-active agents. Also utilized in the synthesis of conjugated materials for medicinal chemistry research due to its stability and reactivity profile.
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