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Moclobemide

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Identification
Molecular formula
C13H17ClN2O2S
CAS number
31352-54-0
IUPAC name
2-(5-hydroxy-1H-indol-3-yl)ethylammonium;6-hydroxy-6-oxo-hexanoate
State
State

At room temperature, moclobemide is usually found in a solid state.

Melting point (Celsius)
129.00
Melting point (Kelvin)
402.00
Boiling point (Celsius)
480.00
Boiling point (Kelvin)
753.00
General information
Molecular weight
327.39g/mol
Molar mass
327.3840g/mol
Density
1.5400g/cm3
Appearence

Moclobemide typically appears as a solid crystalline powder.

Comment on solubility

Solubility of 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 6-hydroxy-6-oxo-hexanoate

The solubility characteristics of 2-(5-hydroxy-1H-indol-3-yl)ethylammonium;6-hydroxy-6-oxo-hexanoate are of particular interest due to its complex molecular structure. Various factors contribute to the solubility of this compound:

  • Polarity: The presence of hydroxyl groups in the molecular structure enhances polar interactions, generally increasing solubility in polar solvents like water.
  • Molecular Interactions: Hydrogen bonding capabilities due to hydroxyl groups can promote solubility.
  • pH Sensitivity: The solubility may vary with pH levels as the ammonium group can become protonated or deprotonated.
  • Temperature Influence: Increasing temperature typically enhances solubility for many organic compounds, including this one.

In general, the solubility of this compound can be expected to be moderately high in aqueous solutions, especially given its combination of hydrophilic portions and potential ionic character. However, empirical data would be essential for precise solubility values. It is important to consider that solubility can greatly affect the bioavailability and reactivity of the compound in various applications.

Interesting facts

Interesting Facts about 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 6-hydroxy-6-oxo-hexanoate

This compound, with its unique structure, offers a fascinating glimpse into the interplay between organic chemistry and biological systems. Here are some intriguing facts about it:

  • Biological Significance: The presence of the indole moiety (5-hydroxy-1H-indole) suggests potential roles in biological processes, as indoles are often found in natural compounds and can participate in various biochemical pathways.
  • Ammonium Ion: The ammonium group in this compound can contribute to its solubility and reactivity, making it a potential candidate for interactions with biological macromolecules, such as proteins and nucleic acids.
  • Potential Applications: Compounds like this one may have applications in drug design, particularly in targeting pathways related to neurotransmission and other neurological functions, due to the indole's structural similarity to neurotransmitters.
  • Oxidative Metabolism: The presence of the 6-hydroxy-6-oxo-hexanoate fragment may indicate that this compound could engage in oxidative metabolic pathways, which are crucial for cellular energy production and regulation.
  • Research Insights: Scientists are continually exploring the synthesis and modification of compounds like this one to uncover their potential therapeutic benefits or to enhance their efficacy in existing pharmaceutical applications.

In the world of chemistry, compounds like 2-(5-hydroxy-1H-indol-3-yl)ethylammonium; 6-hydroxy-6-oxo-hexanoate serve as reminders of how intricate connections can be formed between small molecules and large biological systems. The exploration of such compounds not only enriches the field of chemistry but also inspires innovation in medical and environmental science.

Synonyms
2-(5-hydroxy-1H-indol-3-yl)ethylazanium;6-hydroxy-6-oxohexanoate
UNII-AAJ8D63BQY
INDOL-5-OL, 3-(2-AMINOETHYL)-, ADIPATE
AKOS024360154
ST50989953
3-(2-aminoethyl)indol-5-ol, hexanedioic acid
2-(5-Hydroxy-1H-indol-3-yl)ethanaminium 3-carboxypropanoate