S-Alkylcysteine

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Identification

Molecular formula
C5H10ClNO2S
CAS Number
82419-36-1
IUPAC Name
2-amino-3-(2-chloroethylsulfanyl)propanoic acid
Molecular Weight
183.67g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5360g/cm3
Synonyms
S-(2-Chloroethyl)cysteine
Interesting facts

Interesting Facts about 2-amino-3-(2-chloroethylsulfanyl)propanoic acid

2-amino-3-(2-chloroethylsulfanyl)propanoic acid, commonly known in scientific literature for its unique structure and properties, is a fascinating compound that has captured the interest of chemists. Here are some intriguing aspects:

  • Amine and Acid Properties: This compound contains both an amine group and a carboxylic acid group, making it a versatile building block. Such dual functionality allows for various chemical reactions and applications in synthesis.
  • Biological Relevance: The presence of the sulfenyl group introduces the possibility of interaction with biological systems, raising interesting questions about its potential biological activity and pharmacological applications.
  • Chirality: The 3-position of this compound introduces chirality, leading to the existence of enantiomers. The study of these can provide insights into molecular interactions and the importance of stereochemistry in biological activity.
  • Synthetic Applications: Researchers value this compound in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique functional groups can serve as intermediates in more complex chemical synthesis.
  • Potential Environmental Impact: Compounds like this, especially those containing chlorine, can be studied to understand their environmental impact. It's essential to assess how such chemicals behave in ecological systems.

As evidenced by its multifaceted characteristics, 2-amino-3-(2-chloroethylsulfanyl)propanoic acid holds promise for future research and practical applications, making it a noteworthy subject in the field of chemistry!

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