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Catalog Number:
18425
CAS Number:
72527-77-6
3-Acetyl-4-iodoindole
Synonym(s):
1-(4-Iodo-1H-indol-3-yl)ethanone
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Product Information

3-Acetyl-4-iodoindole is a versatile compound recognized for its significant role in organic synthesis and medicinal chemistry. With its unique structure, this compound serves as a valuable building block in the development of various pharmaceuticals and agrochemicals. Its iodine substituent enhances its reactivity, making it an ideal candidate for further functionalization in complex organic reactions. Researchers have utilized 3-Acetyl-4-iodoindole in the synthesis of indole derivatives, which are known for their diverse biological activities, including anti-cancer and anti-inflammatory properties.

In addition to its applications in drug discovery, this compound is also explored in material science, particularly in the development of organic semiconductors and dyes. Its ability to participate in electronic interactions makes it suitable for creating advanced materials with tailored properties. The compound's stability and ease of handling further contribute to its appeal in both laboratory and industrial settings. Overall, 3-Acetyl-4-iodoindole stands out as a promising compound for researchers seeking innovative solutions in chemistry and materials science.

Synonyms
1-(4-Iodo-1H-indol-3-yl)ethanone
CAS Number
72527-77-6
Molecular Formula
C10H8INO
Molecular Weight
285.08
MDL Number
MFCD04038466
PubChem ID
1514297
Conditions
Store at 0-8°C
General Information
Synonyms
1-(4-Iodo-1H-indol-3-yl)ethanone
CAS Number
72527-77-6
Molecular Formula
C10H8INO
Molecular Weight
285.08
MDL Number
MFCD04038466
PubChem ID
1514297
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

3-Acetyl-4-iodoindole is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to interact with specific biological pathways.
  • Organic Synthesis: It is employed in organic chemistry for creating complex molecules, allowing researchers to explore new compounds with potential applications in drug discovery and material science.
  • Biological Research: The compound is used in studies investigating the effects of indole derivatives on cellular processes, helping scientists understand mechanisms of action in cancer and other diseases.
  • Material Science: 3-Acetyl-4-iodoindole is explored for its properties in developing new materials, including organic semiconductors, which are crucial for advancements in electronic devices.
  • Fluorescent Probes: Its unique structure makes it suitable for designing fluorescent probes, aiding in imaging techniques that enhance the visualization of biological samples in research settings.

Citations