tert-Butyl (2-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)sulfonamido)ethyl)carbamate

95%

  • Product Code: 131769
  CAS:    1014613-14-9
Molecular Weight: 426.34 g./mol Molecular Formula: C₁₉H₃₁BN₂O₆S
EC Number: MDL Number: MFCD28128481
Melting Point: Boiling Point:
Density: 1.19±0.1 g/cm3(Predicted) Storage Condition: 2-8°C, sealed, dry
Product Description: Used primarily as an intermediate in pharmaceutical synthesis, especially in the development of protease inhibitors and other bioactive molecules. Its structure contains both a sulfonamide group and a boronic ester, making it valuable in Suzuki-Miyaura cross-coupling reactions for constructing biaryl systems. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step syntheses. Commonly employed in the preparation of enzyme inhibitors, including those targeting serine proteases, due to the ability of the boron-containing moiety to interact with active site residues. Also utilized in medicinal chemistry for the generation of analogs in structure-activity relationship studies.
Sizes / Availability / Pricing:
Size Availability Price Quantity
100mg 10-20 days ฿2,100.00
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-
250mg 10-20 days ฿3,560.00
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-
1g 10-20 days ฿9,600.00
+
-
tert-Butyl (2-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)sulfonamido)ethyl)carbamate
Used primarily as an intermediate in pharmaceutical synthesis, especially in the development of protease inhibitors and other bioactive molecules. Its structure contains both a sulfonamide group and a boronic ester, making it valuable in Suzuki-Miyaura cross-coupling reactions for constructing biaryl systems. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step syntheses. Commonly employed in the preparation of enzyme inhibitors, including those targeting serine proteases, due to the ability of the boron-containing moiety to interact with active site residues. Also utilized in medicinal chemistry for the generation of analogs in structure-activity relationship studies.
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