2-(dimethylamino)-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethane-1-sulfonamide

95%

Reagent Code: #218332
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CAS Number 756520-90-8

science Other reagents with same CAS 756520-90-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 354.27258 g/mol
Formula C₁₆H₂₇BN₂O₄S
badge Registry Numbers
MDL Number MFCD31916435
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in constructing complex aromatic systems. The sulfonamide and dimethylamino functionalities enhance solubility and provide sites for further modification, useful in medicinal chemistry for designing bioactive molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿16,000.00
250mg
10-20 days ฿40,000.00
1g
10-20 days ฿80,000.00
2-(dimethylamino)-N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethane-1-sulfonamide
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Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in constructing complex aromatic systems. The sulfonamide and dimethylamino functionalities enhance solubility and provide sites for further modification, useful in medicinal chemistry for designing bioactive molecules.
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