N-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine-1-carboxamide

95%

Reagent Code: #215666
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CAS Number 874299-01-1

science Other reagents with same CAS 874299-01-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 330.23 g/mol
Formula C₁₈H₂₇BN₂O₃
badge Registry Numbers
MDL Number MFCD20231465
thermostat Physical Properties
Boiling Point 511.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.12±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive compounds and functional materials. Commonly employed in late-stage functionalization due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,930.00
inventory 1g
10-20 days ฿13,300.00

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N-(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine-1-carboxamide
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive compounds and functional materials. Commonly employed in late-stage functionalization due to its stability and reactivity profile.

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive compounds and functional materials. Commonly employed in late-stage functionalization due to its stability and reactivity profile.

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