(3-(N-Butylsulfamoyl)phenyl)boronic acid

95%

Reagent Code: #215924
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CAS Number 871329-78-1

science Other reagents with same CAS 871329-78-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.11 g/mol
Formula C₁₀H₁₆BNO₄S
badge Registry Numbers
MDL Number MFCD07783858
thermostat Physical Properties
Melting Point 92-94 °C
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonyl-containing drugs. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl systems for drug discovery. Commonly applied in the preparation of bioactive molecules and targeted therapies, especially in oncology and metabolic disease research. Also utilized in the design of sensors and functional materials due to its selective binding properties with diols and other Lewis bases.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,790.00
1g
10-20 days ฿6,980.00
5g
10-20 days ฿20,950.00
(3-(N-Butylsulfamoyl)phenyl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonyl-containing drugs. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl systems for drug discovery. Commonly applied in the preparation of bioactive molecules and targeted therapies, especially in oncology and metabolic disease research. Also utilized in the design of sensors and functional materials due t

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonyl-containing drugs. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl systems for drug discovery. Commonly applied in the preparation of bioactive molecules and targeted therapies, especially in oncology and metabolic disease research. Also utilized in the design of sensors and functional materials due to its selective binding properties with diols and other Lewis bases.

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