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Catalog Number:
20921
CAS Number:
208645-53-8
5-Fluoro-3-(2-nitrovinil)indol
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$97.75 /250 mg
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Product Information

5-Fluoro-3-(2-nitrovinyl)indole is a versatile compound with significant potential in pharmaceutical research and development. This indole derivative features a unique nitrovinyl group, which enhances its reactivity and opens avenues for various synthetic applications. Its structural characteristics make it a valuable intermediate in the synthesis of bioactive molecules, particularly in the development of novel anticancer agents and other therapeutic compounds. Researchers have noted its potential in targeting specific biological pathways, making it a promising candidate for drug discovery.

In addition to its pharmaceutical applications, 5-Fluoro-3-(2-nitrovinyl)indole can be utilized in materials science, particularly in the development of organic electronic devices and sensors. Its ability to participate in various chemical reactions allows for the creation of functionalized materials with tailored properties. This compound stands out due to its unique combination of fluorine and nitro groups, which can enhance the electronic properties of the resulting materials. Overall, 5-Fluoro-3-(2-nitrovinyl)indole offers exciting possibilities for researchers and industry professionals looking to innovate in drug development and advanced materials.

CAS Number
208645-53-8
Molecular Formula
C10H7FN2O2
Molecular Weight
206.18
MDL Number
MFCD00047179
PubChem ID
2774669
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
208645-53-8
Molecular Formula
C10H7FN2O2
Molecular Weight
206.18
MDL Number
MFCD00047179
PubChem ID
2774669
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

5-Fluoro-3-(2-nitrovinyl)indole is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of novel pharmaceuticals, particularly those targeting cancer and neurological disorders, due to its unique structural properties.
  • Organic Synthesis: It is employed in various organic reactions, such as cross-coupling and cycloaddition, allowing chemists to create complex molecules efficiently.
  • 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 development of advanced materials, including polymers and coatings, which benefit from its chemical stability and reactivity.
  • Research on Nitric Oxide Donors: The compound is investigated for its potential as a nitric oxide donor, which may have implications in cardiovascular research and therapies.

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