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

98%

Reagent Code: #214679
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CAS Number 1073353-64-6

science Other reagents with same CAS 1073353-64-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.18 g/mol
Formula C₁₆H₂₄BNO₄
badge Registry Numbers
MDL Number MFCD09266187
thermostat Physical Properties
Melting Point 93-98 °C
Boiling Point 448.2±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.08±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

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 boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl and heterobiaryl systems. Its amide functionality provides a handle for further derivatization or incorporation into larger molecular frameworks. Due to the stability and reactivity profile, it is favored in late-stage functionalization during drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,710.00
inventory 1g
10-20 days ฿4,260.00
inventory 5g
10-20 days ฿12,730.00

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N-(2-Methoxyethyl)-3-(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 boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable for constructing biaryl and heterobiaryl systems. Its amide functionality provides a handle for further derivatization or incorporation into larger molecular frameworks. Due to the stability and reactivity profile, it is favored in late-stage functionalization during drug discovery.
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