3-(2-AMINOETHYL)-4-FLUOROINDOLE

≥98%

  • Product Code: 44240
  CAS:    467452-26-2
Molecular Weight: 178.21 g./mol Molecular Formula: C₁₀H₁₁FN₂
EC Number: MDL Number:
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Density: Storage Condition: 2-8℃, dry
Product Description: This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its structural features, which make it a valuable intermediate in the synthesis of biologically active molecules. Its indole core, combined with the aminoethyl and fluorine substituents, allows it to serve as a building block for developing potential therapeutic agents, particularly in the design of serotonin receptor modulators. These modulators are explored for their potential in treating neurological and psychiatric disorders, such as depression, anxiety, and schizophrenia. Additionally, the presence of the fluorine atom enhances the compound's metabolic stability and binding affinity, making it a useful scaffold in drug discovery programs. Researchers also investigate its role in the development of fluorescent probes for biochemical studies, leveraging its unique chemical properties for imaging and diagnostic applications.
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Size (g) Availability Price Quantity
0.100 10-20 days £325.68
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3-(2-AMINOETHYL)-4-FLUOROINDOLE
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its structural features, which make it a valuable intermediate in the synthesis of biologically active molecules. Its indole core, combined with the aminoethyl and fluorine substituents, allows it to serve as a building block for developing potential therapeutic agents, particularly in the design of serotonin receptor modulators. These modulators are explored for their potential in treating neurological and psychiatric disorders, such as depression, anxiety, and schizophrenia. Additionally, the presence of the fluorine atom enhances the compound's metabolic stability and binding affinity, making it a useful scaffold in drug discovery programs. Researchers also investigate its role in the development of fluorescent probes for biochemical studies, leveraging its unique chemical properties for imaging and diagnostic applications.
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