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

95%

Reagent Code: #215865
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CAS Number 2828444-22-8

science Other reagents with same CAS 2828444-22-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.24 g/mol
Formula C₁₆H₂₄BNO₄S
badge Registry Numbers
MDL Number MFCD29110012
thermostat Physical Properties
Boiling Point 467.3±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.21±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. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Its sulfonamide moiety enhances solubility and stability in various solvents, making it suitable for high-throughput screening and parallel synthesis. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,630.00
inventory 250mg
10-20 days ฿4,450.00
inventory 1g
10-20 days ฿12,990.00

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N-Cyclopropyl-3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
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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. The presence of the boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Its sulfonamide moiety enhances solubility and stability in various solvents, making it suitable for high-throughput screening and parallel synthesis. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required.
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