(4-(N-(3-Methylbutanoyl)sulfamoyl)phenyl)boronic acid

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Reagent Code: #219954
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CAS Number 957120-81-9

science Other reagents with same CAS 957120-81-9

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scatter_plot Molecular Information
Weight 285.1 g/mol
Formula C₁₁H₁₆BNO₅S
badge Registry Numbers
MDL Number MFCD09800865
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in the preparation of enzyme inhibitors, especially those targeting serine proteases, due to the ability of boronic acids to form reversible covalent interactions with active site residues. Also utilized in the design of sensors and functional materials where selective binding or catalytic activity is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,840.00
inventory 250mg
10-20 days ฿4,820.00
inventory 1g
10-20 days ฿13,000.00

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(4-(N-(3-Methylbutanoyl)sulfamoyl)phenyl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in the preparation of enzyme inhibitors, especially those targeting serine proteases, due to the ability of boronic acids to form reversible covalent inter

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in the preparation of enzyme inhibitors, especially those targeting serine proteases, due to the ability of boronic acids to form reversible covalent interactions with active site residues. Also utilized in the design of sensors and functional materials where selective binding or catalytic activity is required.

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