4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

98%

Reagent Code: #87438
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CAS Number 214360-51-7

science Other reagents with same CAS 214360-51-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.15 g/mol
Formula C₁₂H₁₈BNO₄S
badge Registry Numbers
MDL Number MFCD06657806
thermostat Physical Properties
Boiling Point 427.143°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.24±0.1 g/cm3(Predicted)
Storage Room temperature, avoid light, store in inert gas

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex molecules, including pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is utilized in the preparation of sulfonamide-based compounds, which have applications in antibacterial and anti-inflammatory agents. Its stability and reactivity make it a preferred choice in medicinal chemistry for designing bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,107.00
inventory 250mg
10-20 days ฿2,277.00
inventory 1g
10-20 days ฿4,986.00

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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
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This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex molecules, including pharmaceuticals and agrochemicals. Its boronate ester group enables efficient coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is utilized in the preparation of sulfonamide-based compounds, which have applications in antibacterial and anti-inflammatory agents. Its stability and reactivity make it a preferred choice in medicinal chemistry for designing bioactive molecules.
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