Cysteine

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Identification

Molecular formula
C3H7NO2S
CAS Number
52-90-4
IUPAC Name
2-acetamido-3-sulfanyl-propanoic acid
Molecular Weight
121.16g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5300g/cm3
Synonyms
N-Acetyl-DL-cysteine
Interesting facts

Interesting Facts about 2-Acetamido-3-sulfanyl-propanoic acid

2-Acetamido-3-sulfanyl-propanoic acid, often referred to as a unique amino acid derivative, is a compound of significant interest in biological and medicinal chemistry. Here are some engaging facts about this intriguing compound:

  • Biological Role: This compound is known to play a role in various biological processes. The sulfanyl (or thiol) group can participate in redox reactions, making it a potential player in cellular signaling and metabolism.
  • Potential Therapeutic Applications: Researchers are exploring the therapeutic potential of this compound in treating conditions related to oxidative stress due to its unique structure and reactivity.
  • Analytical Chemistry: The presence of both the acetamido and sulfanyl groups makes this compound a subject of interest in analytical chemistry, particularly in the development of sensitive detection methods.
  • Chirality: The compound's structure suggests that it may exist in enantiomeric forms, providing fascinating avenues for studying stereochemistry and its effects on biological activity.
  • Environmental Relevance: Compounds like this are studied to understand their behavior and transformation in the environment, particularly concerning sulfur cycles and organic pollution.

In summary, 2-acetamido-3-sulfanyl-propanoic acid is more than just a chemical compound; it serves as a bridge between fundamental chemistry and its applications in health and environmental sciences. As noted by scientists, "Understanding these compounds unlocks new pathways in therapeutic research."

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