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

98%

Reagent Code: #219264
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CAS Number 1073353-47-5

science Other reagents with same CAS 1073353-47-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.18 g/mol
Formula C₁₃H₂₀BNO₄S
badge Registry Numbers
MDL Number MFCD06657895
inventory_2 Storage & Handling
Storage 2-8°C, Inert gas storage

description Product Description

Used primarily in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its sulfonamide group enhances stability and influences solubility, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the N-methyl and sulfonamide functionalities allows for further functionalization or improved pharmacokinetic properties in target compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,050.00
N-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
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Used primarily in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its sulfonamide group enhances stability and influences solubility, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the N-methyl and sulfonamide functionalities allows for further functionalization or im

Used primarily in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its sulfonamide group enhances stability and influences solubility, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the N-methyl and sulfonamide functionalities allows for further functionalization or improved pharmacokinetic properties in target compounds.

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