(4-(propylsulfonamidomethyl)phenyl)boronic acid

95%

Reagent Code: #226469
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CAS Number 2246874-27-9

science Other reagents with same CAS 2246874-27-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.11434 g/mol
Formula C₁₀H₁₆BNO₄S
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for selective transformations under mild conditions, making it valuable in the preparation of biaryl compounds and functionalized aromatic systems. The sulfonamide group enhances solubility and can participate in hydrogen bonding, useful in medicinal chemistry for designing enzyme inhibitors or bioactive molecules. Also applied in materials science for constructing conjugated systems in organic electronics.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿12,000.00
1g
10-20 days ฿36,000.00
(4-(propylsulfonamidomethyl)phenyl)boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for selective transformations under mild conditions, making it valuable in the preparation of biaryl compounds and functionalized aromatic systems. The sulfonamide group enhances solubility and can participate in hydrogen bonding, useful in medicinal chemistry for designing enzyme inhi

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for selective transformations under mild conditions, making it valuable in the preparation of biaryl compounds and functionalized aromatic systems. The sulfonamide group enhances solubility and can participate in hydrogen bonding, useful in medicinal chemistry for designing enzyme inhibitors or bioactive molecules. Also applied in materials science for constructing conjugated systems in organic electronics.

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