1-Cyclobutyl-6-difluoromethoxy-1H-indole-3-carbonitrile

≥95%

  • Product Code: 80552
  CAS:    1248585-30-9
Molecular Weight: 262.25 g./mol Molecular Formula: C₁₄H₁₂F₂N₂O
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structural features, including the cyclobutyl group and difluoromethoxy moiety, make it a valuable building block for developing potential drug candidates, particularly in the area of kinase inhibitors. These inhibitors are often explored for treating various diseases, including cancer and inflammatory disorders. Additionally, the indole core structure of this compound is frequently employed in the design of compounds targeting neurological conditions, such as depression or anxiety, due to its ability to interact with serotonin receptors. Its carbonitrile group further enhances its utility by providing a reactive site for further chemical modifications, enabling the creation of diverse derivatives for pharmacological screening.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.010 10-20 days ฿5,580.00
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-
0.050 10-20 days ฿16,560.00
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1-Cyclobutyl-6-difluoromethoxy-1H-indole-3-carbonitrile
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structural features, including the cyclobutyl group and difluoromethoxy moiety, make it a valuable building block for developing potential drug candidates, particularly in the area of kinase inhibitors. These inhibitors are often explored for treating various diseases, including cancer and inflammatory disorders. Additionally, the indole core structure of this compound is frequently employed in the design of compounds targeting neurological conditions, such as depression or anxiety, due to its ability to interact with serotonin receptors. Its carbonitrile group further enhances its utility by providing a reactive site for further chemical modifications, enabling the creation of diverse derivatives for pharmacological screening.
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