6-[(1-Hydroxy-1,3-dihydro-2,1-benzoxaborol-5-yl)oxy]nicotinonitrile

95%

  • Product Code: 58398
  CAS:    943311-33-9
Molecular Weight: 252.03 g./mol Molecular Formula: C₁₃H₉BN₂O₃
EC Number: MDL Number:
Melting Point: Boiling Point: 442.5±55.0 °C(Predicted)
Density: 1.38±0.1 g/cm3(Predicted) Storage Condition: 2-8℃
Product Description: This compound is primarily utilized in the development of pharmaceuticals, particularly as an intermediate in the synthesis of novel therapeutic agents. Its unique structure, combining a benzoxaborole moiety with a nicotinonitrile group, makes it valuable for designing molecules with potential biological activity. It is often explored in the research of anti-inflammatory, antifungal, and antibacterial drugs due to the known pharmacological properties of benzoxaborole derivatives. Additionally, it may be investigated for its potential use in treating metabolic disorders or as a building block in medicinal chemistry for creating targeted inhibitors of specific enzymes or pathways. Its application is largely confined to preclinical research and drug discovery efforts.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.001 10-20 days €280.18
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0.005 10-20 days €1,139.70
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6-[(1-Hydroxy-1,3-dihydro-2,1-benzoxaborol-5-yl)oxy]nicotinonitrile
This compound is primarily utilized in the development of pharmaceuticals, particularly as an intermediate in the synthesis of novel therapeutic agents. Its unique structure, combining a benzoxaborole moiety with a nicotinonitrile group, makes it valuable for designing molecules with potential biological activity. It is often explored in the research of anti-inflammatory, antifungal, and antibacterial drugs due to the known pharmacological properties of benzoxaborole derivatives. Additionally, it may be investigated for its potential use in treating metabolic disorders or as a building block in medicinal chemistry for creating targeted inhibitors of specific enzymes or pathways. Its application is largely confined to preclinical research and drug discovery efforts.
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