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Catalog Number:
20531
CAS Number:
76315-55-4
6-Fluoro-3-piperidin-4-yl-1H-indole
Synonym(s):
6-Fluoro-3-(4-piperidinyl)-1H-indole
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Product Information

6-Fluoro-3-piperidin-4-yl-1H-indole is a versatile compound that has garnered attention in pharmaceutical research and development due to its unique structural features and biological activity. This compound, characterized by the presence of a fluorine atom and a piperidine ring, is often explored for its potential applications in medicinal chemistry, particularly in the design of novel therapeutic agents. Its ability to interact with various biological targets makes it a valuable candidate for drug discovery, especially in the fields of neuropharmacology and oncology. Researchers have noted its promising effects in modulating neurotransmitter systems, which could lead to advancements in treatments for neurological disorders.

In addition to its pharmaceutical applications, 6-Fluoro-3-piperidin-4-yl-1H-indole is also utilized in the synthesis of complex organic molecules, making it an essential building block in chemical research. Its stability and reactivity allow for diverse modifications, enabling chemists to tailor compounds for specific functions. This compound stands out among similar indole derivatives due to its unique fluorinated structure, which can enhance bioavailability and efficacy in drug formulations. As the demand for innovative therapeutic solutions continues to rise, 6-Fluoro-3-piperidin-4-yl-1H-indole presents significant potential for researchers and industry professionals alike.

Synonyms
6-Fluoro-3-(4-piperidinyl)-1H-indole
CAS Number
76315-55-4
Molecular Formula
C13H15FN2
Molecular Weight
218.27
MDL Number
MFCD04114735
PubChem ID
11096077
Conditions
Store at 0-8°C
General Information
Synonyms
6-Fluoro-3-(4-piperidinyl)-1H-indole
CAS Number
76315-55-4
Molecular Formula
C13H15FN2
Molecular Weight
218.27
MDL Number
MFCD04114735
PubChem ID
11096077
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Fluoro-3-piperidin-4-yl-1H-indole is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing new treatments for neurological disorders.
  • Neuroscience Research: Its unique structure allows researchers to explore its effects on neurotransmitter systems, aiding in the understanding of brain function and potential therapies for mental health conditions.
  • Drug Discovery: The compound is valuable in high-throughput screening processes, helping scientists identify promising drug candidates more efficiently.
  • Biochemical Studies: It is used in studying receptor interactions, providing insights into drug-receptor dynamics that can lead to more effective medications.
  • Material Science: Beyond pharmaceuticals, this chemical can be explored for its potential applications in developing advanced materials, leveraging its unique chemical properties.

Citations