N-Cyclopropyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

98%

Reagent Code: #219938
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CAS Number 914610-50-7

science Other reagents with same CAS 914610-50-7

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. The sulfonamide moiety enhances solubility and can serve as a directing or stabilizing group in molecular design. Its cyclopropyl group contributes to metabolic stability in drug candidates, increasing its utility in medicinal chemistry for developing bioactive compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿710.00
inventory 1g
10-20 days ฿2,340.00
inventory 5g
10-20 days ฿11,530.00
inventory 25g
10-20 days ฿57,650.00
N-Cyclopropyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. The sulfonamide moiety enhances solubility and can serve as a directing or stabilizing group in molecular design. Its cyclopropyl group contribute

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings, making it valuable in pharmaceutical and agrochemical research for constructing biaryl systems. The sulfonamide moiety enhances solubility and can serve as a directing or stabilizing group in molecular design. Its cyclopropyl group contributes to metabolic stability in drug candidates, increasing its utility in medicinal chemistry for developing bioactive compounds.

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