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

95%

Reagent Code: #215864
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CAS Number 2828443-89-4

science Other reagents with same CAS 2828443-89-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 343.27 g/mol
Formula C₂₀H₃₀BNO₃
thermostat Physical Properties
Boiling Point 483.0±28.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.07±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical research. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild palladium-catalyzed conditions. Its amide functionality provides structural stability and polarity, making it valuable for constructing bioactive molecules and functional materials. Due to its well-defined reactivity, it is often employed in late-stage functionalization during drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,880.00
inventory 250mg
10-20 days ฿3,180.00
inventory 1g
10-20 days ฿8,580.00

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N-Cyclohexyl-N-methyl-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 complex organic molecules, especially in pharmaceutical and agrochemical research. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild palladium-catalyzed conditions. Its amide functionality provides structural stability and polarity, making it valuable for constructing bioactive molecules and functional materials. Due to its well-defined re
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical research. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild palladium-catalyzed conditions. Its amide functionality provides structural stability and polarity, making it valuable for constructing bioactive molecules and functional materials. Due to its well-defined reactivity, it is often employed in late-stage functionalization during drug discovery and development.
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