N-Cyclopentyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

95%

Reagent Code: #215922
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CAS Number 933987-10-1

science Other reagents with same CAS 933987-10-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.22 g/mol
Formula C₁₈H₂₆BNO₃
badge Registry Numbers
MDL Number MFCD16660857
thermostat Physical Properties
Boiling Point 470.7±28.0 °C(Predicted)
inventory_2 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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,020.00
1g
10-20 days ฿2,740.00
5g
10-20 days ฿9,590.00
N-Cyclopentyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
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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
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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