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Catalog Number:
21407
CAS Number:
114305-99-6
6-Chloro-3-indolyl acetate
Synonym(s):
6-Chloro-1H-indol-3-yl acetate
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Product Information

6-Chloro-3-indolyl acetate is a versatile chemical compound widely recognized for its applications in biochemical research and pharmaceutical development. This compound, a derivative of indole, is particularly valued for its role as a substrate in enzyme assays and as a building block in the synthesis of various bioactive molecules. Its unique structure allows it to participate in diverse chemical reactions, making it an essential tool for researchers exploring indole-based compounds and their derivatives.

In the pharmaceutical industry, 6-Chloro-3-indolyl acetate has shown promise in the development of novel therapeutic agents, particularly in the fields of oncology and neurology. Its ability to modulate biological pathways makes it a candidate for further investigation in drug discovery programs. Additionally, this compound can be utilized in the synthesis of fluorescent probes, enhancing its utility in biological imaging and diagnostics. With its favorable properties and broad applicability, 6-Chloro-3-indolyl acetate stands out as a valuable asset for researchers and industry professionals alike.

Synonyms
6-Chloro-1H-indol-3-yl acetate
CAS Number
114305-99-6
Molecular Formula
C10H8ClNO2
Molecular Weight
209.63
MDL Number
MFCD00269776
PubChem ID
18955884
Conditions
Store at 0-8°C
General Information
Synonyms
6-Chloro-1H-indol-3-yl acetate
CAS Number
114305-99-6
Molecular Formula
C10H8ClNO2
Molecular Weight
209.63
MDL Number
MFCD00269776
PubChem ID
18955884
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-Chloro-3-indolyl acetate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a valuable intermediate in the synthesis of various pharmaceuticals, particularly in developing anti-cancer agents due to its ability to interact with biological targets effectively.
  • Biochemical Research: It is used in studies investigating enzyme activity and protein interactions, helping researchers understand cellular processes and develop new therapeutic strategies.
  • Agricultural Chemistry: The compound is explored for its potential as a plant growth regulator, promoting healthier plant development and improving crop yields, which is crucial for sustainable agriculture.
  • Material Science: 6-Chloro-3-indolyl acetate is investigated for its applications in creating novel materials, particularly in the field of organic electronics, where it can enhance the performance of devices.
  • Diagnostic Tools: Its properties make it suitable for developing diagnostic assays, aiding in the detection of specific biomolecules, which is essential for medical diagnostics and research.

Citations