N-Cyclopropyl-3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
95%
Reagent
Code: #215865
CAS Number
2828444-22-8
blur_circular Chemical Specifications
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Molecular Information
Weight
337.24 g/mol
Formula
C₁₆H₂₄BNO₄S
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Registry Numbers
MDL Number
MFCD29110012
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Physical Properties
Boiling Point
467.3±55.0 °C(Predicted)
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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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