N-Cyclopentyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
95%
Reagent
Code: #215922
CAS Number
933987-10-1
science Other reagents with same CAS 933987-10-1
blur_circular Chemical Specifications
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Molecular Information
Weight
315.22 g/mol
Formula
C₁₈H₂₆BNO₃
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Registry Numbers
MDL Number
MFCD16660857
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Physical Properties
Boiling Point
470.7±28.0 °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 primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. The presence of the boronate ester group enables efficient carbon-carbon bond formation under palladium catalysis, allowing for the construction of complex aromatic systems. Its amide functionality provides a handle for further derivatization, making it valuable in medicinal chemistry for developing bioactive molecules. The cyclopentyl group contributes to steric and metabolic stability, which is beneficial in drug design. It is particularly useful in late-stage functionalization due to its compatibility with a variety of functional groups and reaction conditions.
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