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Catalog Number:
21687
CAS Number:
2795-41-7
6-Fluoroindol-3-carboxaldehído
Purity:
≥ 98 % (HPLC)
Synonym(s):
6-Fluoroindol-3-aldehído, 6-Fluoroindol-3-carbaldehído
Documents
$22.03 /1G
Tamaño
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Product Information

6-Fluoroindole-3-carboxaldehyde is a versatile compound with significant applications in medicinal chemistry and organic synthesis. This compound, characterized by its unique fluorine substitution, enhances the reactivity of the indole structure, making it an essential building block for the development of various pharmaceuticals. Its aldehyde functional group allows for further functionalization, facilitating the synthesis of complex molecules. Researchers have utilized 6-Fluoroindole-3-carboxaldehyde in the design of novel drug candidates, particularly in the development of anti-cancer and anti-inflammatory agents.

In addition to its pharmaceutical applications, this compound serves as a valuable intermediate in the synthesis of fluorescent dyes and agrochemicals. Its ability to undergo various chemical transformations makes it a preferred choice for chemists looking to innovate in fields such as materials science and biochemistry. With its unique properties and broad applicability, 6-Fluoroindole-3-carboxaldehyde stands out as a crucial compound for researchers and industry professionals aiming to push the boundaries of chemical synthesis and drug discovery.

Synonyms
6-Fluoroindol-3-aldehído, 6-Fluoroindol-3-carbaldehído
CAS Number
2795-41-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C9H6FNO
Molecular Weight
163.15
MDL Number
MFCD00069703
PubChem ID
262903
Melting Point
170-176 ?C
Appearance
Polvo cristalino amarillo
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
6-Fluoroindol-3-aldehído, 6-Fluoroindol-3-carbaldehído
CAS Number
2795-41-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C9H6FNO
Molecular Weight
163.15
MDL Number
MFCD00069703
PubChem ID
262903
Melting Point
170-176 ?C
Appearance
Polvo cristalino amarillo
Conditions
Conservar entre 0 y 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-Fluoroindole-3-carboxaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of novel anti-cancer agents due to its ability to interact with biological targets effectively.
  • Organic Synthesis: It is employed in the synthesis of complex organic molecules, allowing chemists to create compounds with specific properties, which can be crucial for drug discovery and development.
  • Fluorescent Probes: The compound can be used to develop fluorescent probes for biological imaging, enhancing the ability to visualize cellular processes in real-time.
  • Material Science: It finds applications in the creation of advanced materials, including polymers and coatings, that require specific chemical properties for improved performance.
  • Research in Neuroscience: 6-Fluoroindole-3-carboxaldehyde is being explored for its potential effects on neurotransmitter systems, which could lead to breakthroughs in understanding and treating neurological disorders.

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