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Catalog Number:
18432
CAS Number:
4769-95-3
3-Acetyl-4-nitroindole
Synonym(s):
1-(4-Nitro-1H-indol-3-yl)ethanone
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Product Information

3-Acetyl-4-nitroindole is a versatile compound recognized for its significant applications in organic synthesis and pharmaceutical research. This compound features a unique structure that combines an acetyl group with a nitro-substituted indole, making it a valuable intermediate in the synthesis of various bioactive molecules. Its ability to participate in diverse chemical reactions, such as electrophilic substitutions and coupling reactions, allows researchers to explore new pathways for drug development and material science.

In the pharmaceutical industry, 3-Acetyl-4-nitroindole has been investigated for its potential as an anti-inflammatory and antimicrobial agent, showcasing its relevance in developing therapeutic agents. Additionally, its unique properties make it suitable for use in dye and pigment formulations, enhancing color stability and performance. Researchers and industry professionals will find this compound beneficial for its multifunctionality and the potential to streamline synthesis processes, ultimately contributing to innovative solutions in their respective fields.

Synonyms
1-(4-Nitro-1H-indol-3-yl)ethanone
CAS Number
4769-95-3
Molecular Formula
C10H8N2O3
Molecular Weight
204.18
MDL Number
MFCD06658294
PubChem ID
11183310
Conditions
Store at 0-8°C
General Information
Synonyms
1-(4-Nitro-1H-indol-3-yl)ethanone
CAS Number
4769-95-3
Molecular Formula
C10H8N2O3
Molecular Weight
204.18
MDL Number
MFCD06658294
PubChem ID
11183310
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-nitroindole is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in creating anti-inflammatory and analgesic agents.
  • Organic Synthesis: It is employed in organic chemistry for the development of novel indole derivatives, which are important in medicinal chemistry due to their diverse biological activities.
  • Biological Research: Researchers use it to study the mechanisms of action of nitroindole derivatives, which can lead to the discovery of new therapeutic agents targeting specific diseases.
  • Material Science: The compound is explored for its potential applications in developing organic electronic materials, such as organic light-emitting diodes (OLEDs), due to its unique electronic properties.
  • Analytical Chemistry: It is utilized as a reference standard in analytical methods, aiding in the detection and quantification of similar compounds in complex mixtures.

Citations