(5-(N-(tert-Butyl)sulfamoyl)pyridin-3-yl)boronic acid

95%

  • Product Code: 37022
  CAS:    1314987-50-2
Molecular Weight: 258.10 g./mol Molecular Formula: C₉H₁₅BN₂O₄S
EC Number: MDL Number: MFCD27955970
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. It is often employed in the development of drug candidates, where it acts as a key intermediate in constructing biologically active compounds. Additionally, its pyridine ring structure provides stability and reactivity, enhancing its utility in medicinal chemistry and material science applications.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $374.49
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0.250 10-20 days $624.72
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1.000 10-20 days $1,660.27
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(5-(N-(tert-Butyl)sulfamoyl)pyridin-3-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. It is often employed in the development of drug candidates, where it acts as a key intermediate in constructing biologically active compounds. Additionally, its pyridine ring structure provides stability and reactivity, enhancing its utility in medicinal chemistry and material science applications.
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