(4-(N,N-Dimethylsulfamoyl)-2-methylphenyl)boronic acid

96%

Reagent Code: #215914
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CAS Number 957034-82-1

science Other reagents with same CAS 957034-82-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.09 g/mol
Formula C₉H₁₄BNO₄S
badge Registry Numbers
MDL Number MFCD09475839
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in organic synthesis as a boronic acid coupling partner in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its sulfamoyl group enhances solubility and can influence electronic properties in pharmaceutical intermediates. Commonly applied in medicinal chemistry for developing sulfonamide-containing drug candidates and in materials science for designing functional organic molecules. Stable under standard conditions and compatible with various functional groups, making it suitable for complex molecule assembly.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿4,330.00
1g
10-20 days ฿11,680.00
5g
10-20 days ฿40,890.00

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(4-(N,N-Dimethylsulfamoyl)-2-methylphenyl)boronic acid
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Used in organic synthesis as a boronic acid coupling partner in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its sulfamoyl group enhances solubility and can influence electronic properties in pharmaceutical intermediates. Commonly applied in medicinal chemistry for developing sulfonamide-containing drug candidates and in materials science for designing functional organic molecules. Stable under standard conditions and compatible

Used in organic synthesis as a boronic acid coupling partner in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds for constructing biaryl compounds. Its sulfamoyl group enhances solubility and can influence electronic properties in pharmaceutical intermediates. Commonly applied in medicinal chemistry for developing sulfonamide-containing drug candidates and in materials science for designing functional organic molecules. Stable under standard conditions and compatible with various functional groups, making it suitable for complex molecule assembly.

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