5-Hydroxytryptamine acetate

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Identification

Molecular formula
C12H14N2O2
CAS Number
50-47-5
IUPAC Name
[3-(2-aminoethyl)-1H-indol-5-yl] acetate
Molecular Weight
176.22g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5830g/cm3
Synonyms
Oprea1_251674
Interesting facts

Interesting Facts about [3-(2-aminoethyl)-1H-indol-5-yl] acetate

[3-(2-aminoethyl)-1H-indol-5-yl] acetate is an intriguing chemical compound that illustrates the fascinating relationship between structure and function in organic chemistry. This compound embodies several key aspects of both biochemical significance and synthetic utility, making it an interesting subject of study.

Key Features

  • Biological Relevance: This compound is a derivative of indole, a structure that is widely known for its occurrence in many biologically active molecules, including neurotransmitters and hormones like serotonin.
  • Potential Applications: Due to its aminoethyl side chain, this compound might exhibit properties useful in drug development, particularly in the fields of neuroscience and pharmacology, as it could help in designing compounds targeting the serotonin receptor system.
  • Synthetic Pathways: The synthesis of [3-(2-aminoethyl)-1H-indol-5-yl] acetate often involves multi-step reactions that highlight key transformations in organic chemistry, such as acetylation and amine coupling. This can serve as a great teaching tool for understanding synthetic strategies.

Quote from Research

As one researcher stated, “The indole scaffold offers a diverse platform for chemical modification, leading to a plethora of compounds with diverse biological activities.” This shows the limitless possibilities for exploration within this class of compounds.

Conclusion

Ultimately, [3-(2-aminoethyl)-1H-indol-5-yl] acetate not only serves as a valuable compound for theoretical studies but could also pave the way for innovations in therapeutic agents. Its intricate structure presents an exciting opportunity for chemists to explore and leverage in various scientific fields.

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