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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
State
State

At room temperature, the substance is found in a solid state. It is generally stable under normal conditions of use and storage.

Melting point (Celsius)
198.00
Melting point (Kelvin)
471.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
176.22g/mol
Molar mass
176.2150g/mol
Density
1.5830g/cm3
Appearence

The compound typically appears as an off-white to pale pink crystalline powder.

Comment on solubility

Solubility of [3-(2-aminoethyl)-1H-indol-5-yl] acetate

The compound [3-(2-aminoethyl)-1H-indol-5-yl] acetate, with its complex indole structure, displays interesting solubility characteristics. Here are some important points regarding its solubility:

  • Polar and Non-Polar Influence: The presence of both the indole structure and the acetate functional group suggests that this compound may have both polar and non-polar characteristics, impacting its solubility in different solvents.
  • Water Solubility: Given that the acetate moiety can engage in hydrogen bonding, the compound may exhibit moderate solubility in polar solvents such as water. However, the hydrophobic indole ring could limit this solubility.
  • Solvent Compatibility: It is likely to be more soluble in organic solvents like ethanol or DMSO, where lipophilic interactions can play a significant role.
  • pH Effects: The solubility may vary with changes in pH. In a more acidic or basic environment, the ionization of the amino group could enhance solubility in aqueous solutions.

In summary, solubility can be influenced by several factors, including the chemical environment, solvent type, and temperature. As always, empirical data should be consulted for practical applications, as theoretical considerations might not always predict real-world behavior.

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.

Synonyms
Oprea1_251674
SCHEMBL12720798