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3-ethyl-2-methyl-5-(morpholin-4-ium-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one chloride

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Identification
Molecular formula
C18H25ClN2O2
CAS number
123456-78-9
IUPAC name
3-ethyl-2-methyl-5-(morpholin-4-ium-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one;chloride
State
State

At room temperature, it is typically found as a solid, taking the form of crystalline powder or a solid mass.

Melting point (Celsius)
175.00
Melting point (Kelvin)
448.15
Boiling point (Celsius)
456.20
Boiling point (Kelvin)
729.35
General information
Molecular weight
344.85g/mol
Molar mass
344.8500g/mol
Density
1.1800g/cm3
Appearence

The compound appears as an off-white to pale yellow crystalline powder. It may also appear as a solid mass with a homogenous texture.

Comment on solubility

Solubility of 3-ethyl-2-methyl-5-(morpholin-4-ium-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one;chloride

The solubility of the compound 3-ethyl-2-methyl-5-(morpholin-4-ium-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one chloride is influenced by various factors, such as its molecular structure and interactions with solvents. Here are some points to consider regarding its solubility:

  • Chloride Salt Form: As a chloride salt, it generally exhibits increased solubility in polar solvents like water compared to its parent base due to ionization, which facilitates interactions with water molecules.
  • Hydrophilicity: The presence of the morpholinium group enhances its hydrophilicity, contributing to a higher solubility profile in aqueous solutions.
  • Hydrophobic Regions: Despite the hydrophilic features, the molecule also contains hydrophobic aromatic regions, which may create limitations in solubility depending on the solvent's nature.
  • Temperature Dependence: Generally, solubility is influenced by temperature, where an increase may enhance the solubility of this compound in various solvents.

In summary, the solubility of 3-ethyl-2-methyl-5-(morpholin-4-ium-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one; chloride is likely to be favorable in polar solvents, particularly water, but can exhibit variable solubility due to its unique structural characteristics.

Interesting facts

Exploring 3-ethyl-2-methyl-5-(morpholin-4-ium-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one;chloride

This fascinating compound, known as 3-ethyl-2-methyl-5-(morpholin-4-ium-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one;chloride, presents a unique structural framework that offers insight into its potential applications and biological relevance.

Key Characteristics and Relevance

  • Molecular Complexity: The compound features a tetrahydroindole core, which is of significant interest in medicinal chemistry due to its presence in many biologically active molecules.
  • Presence of Morpholine: The morpholine ring contributes to the compound's solubility and biological activity, making it a valuable component in pharmaceutical design.
  • Diverse Applications: Compounds similar to this one have been investigated for their potential in areas such as antimicrobial and antitumor activity.
  • Research Significance: The structural diversity provided by the substituents, such as the ethyl and methyl groups, influences the compound's interaction with biological targets, making it crucial in structure-activity relationship studies.

Potential Impacts in Science

As researchers continue to explore chemical compounds like 3-ethyl-2-methyl-5-(morpholin-4-ium-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one;chloride, the compound serves as a reminder of the intricate relationship between structure and function in drug development. As the famous chemist Linus Pauling once said, "The greatest and most important problems of life are all in a sense insoluble. They can never be solved but only outgrown." This sentiment rings true as scientists strive to unlock the potential of complex molecules like this one.

In conclusion, the ongoing study of such compounds not only enhances our understanding of chemical properties but also opens new avenues for innovation in therapeutic agents.

Synonyms
AKOS026749933
3-ethyl-2-methyl-5-(morpholin-4-ium-4-ylmethyl)-1,5,6,7-tetrahydroindol-4-one;chloride