Skip to main content

2-Amino-3-(1,2-dichlorovinylthio)propanoic acid

ADVERTISEMENT
Identification
Molecular formula
C5H7Cl2NO2S
CAS number
89945-34-2
IUPAC name
2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid
State
State

This compound is solid at room temperature. It remains stable under standard conditions, making it manageable for various analytical and chemical synthesis applications.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.00
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.00
General information
Molecular weight
227.09g/mol
Molar mass
227.0890g/mol
Density
1.4000g/cm3
Appearence

This compound typically appears as a white crystalline solid. Its physical manifestation in a solid state contributes to its handling properties, making it relatively stable under standard conditions.

Comment on solubility

Solubility of 2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid

The solubility of 2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid can be influenced by various factors, making it an interesting compound to analyze. Here are some key points regarding its solubility:

  • Polarity: The presence of polar functional groups in the structure can enhance solubility in polar solvents such as water.
  • Hydrogen Bonding: The amino group (-NH2) may engage in hydrogen bonding, which typically increases solubility in aqueous solutions.
  • Presence of Chlorine Atoms: The dichloro substituents may introduce some steric hindrance and alter the overall solubility in various organic solvents.
  • pH Dependence: As an acid, its solubility can be pH-dependent; it is more likely to be soluble when in its deprotonated (anionic) form at higher pH values.

In summary, the solubility of 2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid is a complex interplay of its structural features and environmental conditions. Understanding these factors is essential for predicting its behavior in different chemical environments.

Interesting facts

Interesting Facts about 2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid

2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid, commonly referred to as a derivative of amino acids, is a compound that garners attention primarily due to its unique structural features and potential functionality. Here are some intriguing points regarding this compound:

  • Structural Complexity: This compound is notable for its dual functionality as both an amino acid and a vinylsulfanyl derivative, highlighting the innovative combinations possible in organic synthesis.
  • Synthetic Utility: The presence of the dichlorovinyl group suggests possible applications in medicinal chemistry, where such functional groups serve as intermediates or key components in drug design.
  • Biological Relevance: Amino acids are the building blocks of proteins. Compounds like this one may offer insights into enzyme activity or metabolic pathways, making them significant in biochemistry.
  • Toxicological Implications: The dichlorovinyl moiety could indicate potential toxicity, and studies regarding the environmental impacts and safety profiles of similar compounds are crucial in chemistry.
  • Quotes from Research: As noted in several studies, “The exploration of sulfanyl derivatives continues to unlock new avenues in both organic and medicinal chemistry.” This illustrates the growing interest in such compounds.

As researchers continue to examine compounds like 2-amino-3-(1,2-dichlorovinylsulfanyl)propanoic acid, the potential applications in drug discovery, environmental science, and green chemistry remain a promising frontier for chemical exploration.

Synonyms
2-amino-3-(1,2-dichloroethenylsulfanyl)propanoic acid
S-(1,2-Dichlorovinyl)-L-cysteine
S-[(1E)-1,2-dichloroethenyl]--L-cysteine
SCHEMBL10598971
s-(1,2-dichloroethenyl)cysteine
DTXSID60871798
13419-46-0