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Captopril Disulfide

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Identification
Molecular formula
C22H28N2O7S2
CAS number
59948-25-5
IUPAC name
2-amino-5-[[1-(benzylsulfanylmethyl)-2-(carboxymethylamino)-2-oxo-ethyl]amino]-5-oxo-pentanoic acid
State
State

At room temperature, it is a solid.

Melting point (Celsius)
97.50
Melting point (Kelvin)
370.65
Boiling point (Celsius)
179.00
Boiling point (Kelvin)
452.15
General information
Molecular weight
548.68g/mol
Molar mass
548.6800g/mol
Density
1.2743g/cm3
Appearence

Captopril Disulfide appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 2-amino-5-[[1-(benzylsulfanylmethyl)-2-(carboxymethylamino)-2-oxo-ethyl]amino]-5-oxo-pentanoic acid

The solubility of 2-amino-5-[[1-(benzylsulfanylmethyl)-2-(carboxymethylamino)-2-oxo-ethyl]amino]-5-oxo-pentanoic acid, with the chemical formula C22H28N2O7S2, can be influenced by several factors due to its complex molecular structure. Understanding its solubility characteristics is essential for its applications in various fields. Consider the following points:

  • Polarity: The presence of functional groups such as amines and carboxylic acids contributes to the compound’s polarity, suggesting potential solubility in polar solvents like water.
  • Hydrophilicity vs. Hydrophobicity: The benzylsulfanylmethyl moiety introduces a hydrophobic character, which may limit the solubility in aqueous solutions.
  • pH Sensitivity: The solubility may vary with pH, particularly due to the carboxymethylamine groups, which can either protonate or deprotonate depending on the pH of the environment.
  • Temperature Influence: Higher temperatures may increase solubility for some compounds, allowing for better dissolution in appropriate solvents.

In summary, the solubility of this compound is likely to be moderate due to its intricate structure that combines both hydrophilic and hydrophobic elements. Factors such as solvent choice, pH level, and temperature should be considered when assessing its behavior in various solutions.

Interesting facts

Interesting Facts about 2-amino-5-[[1-(benzylsulfanylmethyl)-2-(carboxymethylamino)-2-oxo-ethyl]amino]-5-oxo-pentanoic acid

This compound presents a fascinating structure that hints at a multitude of biological applications, particularly in the field of medicinal chemistry. With its complex arrangement, 2-amino-5-[[1-(benzylsulfanylmethyl)-2-(carboxymethylamino)-2-oxo-ethyl]amino]-5-oxo-pentanoic acid is notable for several reasons:

  • Multi-functional Grouping: The presence of both amino and carboxyl groups makes this compound amphoteric, allowing it to interact in a variety of chemical environments.
  • Potential Biological Activity: Compounds similar to this one have been investigated for their roles in pharmaceutical applications, especially in the context of enzyme inhibition and drug design.
  • Sulfide Linkage: The inclusion of a benzylsulfanylmethyl group may impart unique chemical properties, contributing to the compound's solubility and reactivity, which are crucial for its efficacy in biological systems.
  • Structural Complexity: The multi-ring structure and diverse functional groups of this compound provide a platform for investigating structure-activity relationships (SAR), which is essential for drug development.
  • Research Potential: This compound’s structure offers opportunities for exploration in both synthetic and biological chemistry, paving the way for innovation in therapeutic applications and material sciences.

As a student or researcher in chemistry, uncovering the mechanisms by which this compound operates could lead to advancements in healthcare and novel insights into chemical reactivity. In the words of a famed chemist, “The beauty of chemistry lies in the unexpected relationships between structure and function.”

Overall, 2-amino-5-[[1-(benzylsulfanylmethyl)-2-(carboxymethylamino)-2-oxo-ethyl]amino]-5-oxo-pentanoic acid serves as an exemplary case study in the intricate dance of molecular interactions.

Synonyms
SCHEMBL5000996