N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarboxamide

95%

Reagent Code: #218342
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CAS Number 1031747-40-6

science Other reagents with same CAS 1031747-40-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.16178 g/mol
Formula C₁₆H₂₂BNO₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boron-containing group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds. This makes it valuable in constructing biaryl and heterobiaryl systems found in active pharmaceutical ingredients. Additionally, the cyclopropane amide moiety can enhance metabolic stability and binding affinity in drug candidates, making the compound useful in medicinal chemistry for developing bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,400.00
inventory 250mg
10-20 days ฿12,800.00
inventory 1g
10-20 days ฿38,400.00
N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarboxamide
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Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boron-containing group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds. This makes it valuable in constructing biaryl and heterobiaryl systems found in active pharmaceutical ingredients. Additionally, the cyclopropane amide moiety can enhance metabolic stability and binding a

Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boron-containing group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds. This makes it valuable in constructing biaryl and heterobiaryl systems found in active pharmaceutical ingredients. Additionally, the cyclopropane amide moiety can enhance metabolic stability and binding affinity in drug candidates, making the compound useful in medicinal chemistry for developing bioactive molecules.

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