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L-Formylcystine

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Identification
Molecular formula
C7H10N2O5S2
CAS number
3061-88-9
IUPAC name
(2R)-3-[[(2R)-2-(carboxyamino)-3-oxo-propyl]disulfanyl]-2-formamido-propanoic acid
State
State

At room temperature, L-Formylcystine is in a solid state.

Melting point (Celsius)
184.00
Melting point (Kelvin)
457.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
238.27g/mol
Molar mass
238.2660g/mol
Density
1.5152g/cm3
Appearence

L-Formylcystine appears as a white to off-white crystalline powder. It is typically odorless.

Comment on solubility

Solubility of (2R)-3-[[[2R]-2-(carboxyamino)-3-oxo-propyl]disulfanyl]-2-formamido-propanoic acid

The solubility of (2R)-3-[[[2R]-2-(carboxyamino)-3-oxo-propyl]disulfanyl]-2-formamido-propanoic acid can be influenced by several factors:

  • Polarity: The presence of multiple functional groups, including the carboxylic acid and amino groups, suggests a high degree of polarity, which typically enhances solubility in polar solvents like water.
  • pH Dependency: The solubility can vary with pH, especially due to the carboxylic acid group, which can dissociate at elevated pH levels, increasing solubility.
  • Hydrogen Bonding: This compound can engage in hydrogen bonding with water molecules, further promoting solubility in aqueous solutions.

However, the solubility may also be affected by:

  • Temperature: Higher temperatures often increase solubility for many organic compounds.
  • Concentration of Solvent: The presence of other solutes can compete for solvation, affecting the overall solubility.
  • Molecular Structure: The disulfide bond may introduce steric hindrance, potentially impacting solubility, especially in non-polar solvents.

In summary, while this compound is likely soluble in water due to its polar characteristics, the exact solubility can be complex, requiring empirical testing to determine precise values and solubility limits.

Interesting facts

Interesting Facts about (2R)-3-[[(2R)-2-(carboxyamino)-3-oxo-propyl]disulfanyl]-2-formamido-propanoic acid

This unique compound, often referred to in biochemical applications, showcases several fascinating features that highlight its importance in the realm of chemistry:

  • Structure and Function: The compound includes a disulfide bond, which is crucial in protein structure and function, aiding in the stability and integrity of proteins.
  • Biological Importance: It plays a role as a potential inhibitor in various biochemical pathways, making it a subject of interest for researchers in drug design and development.
  • Amino Acid Derivative: As a derivative of amino acids, this compound can be a key player in understanding peptide synthesis and the behavior of related compounds in biological systems.
  • Research Applications: This compound is significant in studies related to antioxidant activity and cellular signaling, which are vital for various metabolic processes.
  • Therapeutic Potential: It is being investigated for its potential therapeutic effects, particularly in conditions related to oxidative stress and cell signaling abnormalities.

In essence, the study of (2R)-3-[[(2R)-2-(carboxyamino)-3-oxo-propyl]disulfanyl]-2-formamido-propanoic acid offers a window into the intricate world of biochemical interactions and therapeutic exploration. As one scientist aptly put it, "Understanding the nuances of such compounds can unlock new frontiers in medicinal chemistry." Through further research, the applications and implications of this compound could broaden our understanding of complex biochemical pathways.

Synonyms
NSC 74466
BRN 1729729
3-04-00-01622 (Beilstein Handbook Reference)