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

≥95%

Reagent Code: #215524
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CAS Number 1228152-57-5

science Other reagents with same CAS 1228152-57-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.23 g/mol
Formula C₁₅H₂₄BNO₄S
thermostat Physical Properties
Boiling Point 432.5±47.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.15±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in constructing complex aromatic compounds. Commonly employed in medicinal chemistry for developing sulfonamide-based bioactive molecules. Stable and compatible with a variety of functional groups, it supports efficient and selective transformations in late-stage functionalization of drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿4,230.00
1g
10-20 days ฿12,340.00
N-Isopropyl-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, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in constructing complex aromatic compounds. Commonly employed in medicinal chemistry for developing sulfonamide-based bioactive molecules. Stable and compatible with a variety of functional groups, it supports efficient and selective transformations in late-stage functionalization of drug candidates.
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