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

95%

Reagent Code: #180888
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CAS Number 756520-45-3

science Other reagents with same CAS 756520-45-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.1889 g/mol
Formula C₁₄H₂₀BNO₄S
badge Registry Numbers
MDL Number MFCD22494224
thermostat Physical Properties
Boiling Point 425.1±47.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl structures. The presence of the sulfonamide moiety adds polarity and stability, which can enhance binding properties in bioactive molecule design. It is particularly useful in medicinal chemistry for developing drug candidates with improved metabolic stability and target selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿40,000.00
inventory 1g
10-20 days ฿82,950.00

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Ethenesulfonamide,N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl structures. The presence of the sulfonamide moiety adds polarity and stability, which can enhance binding properties in bioactive molecule design. It

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for constructing biaryl structures. The presence of the sulfonamide moiety adds polarity and stability, which can enhance binding properties in bioactive molecule design. It is particularly useful in medicinal chemistry for developing drug candidates with improved metabolic stability and target selectivity.

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