Cysteine

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Identification

Molecular formula
C3H7NO2S
CAS Number
52-90-4
IUPAC Name
2-amino-4-(2-amino-2-carboxy-ethyl)sulfanyl-butanoic acid
Molecular Weight
121.16g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3407g/cm3
Appearance
is common for amino acids due to their crystalline nature.
Synonyms
cystathionine
Interesting facts

Interesting Facts about 2-amino-4-(2-amino-2-carboxy-ethyl)sulfanyl-butanoic Acid

2-amino-4-(2-amino-2-carboxy-ethyl)sulfanyl-butanoic acid, commonly referred to as a derivative of a key amino acid, possesses several compelling characteristics that make it intriguing in the realm of biochemistry.

Key Characteristics

  • Structure & Composition: This compound features both amino and carboxylic functional groups, making it a fascinating example of an amino acid derivative.
  • Biological Functions: It plays a role in various biological processes, particularly in metabolic pathways and as a building block for proteins.
  • Potential Applications: Due to its unique structure, this compound may exhibit antioxidant properties and could be explored for its potential in pharmaceutical applications.

Furthermore, it’s noteworthy that the presence of sulfur in its structure allows for interesting redox chemistry, which could lead to significant implications in biochemical reactions. As a scientist or chemistry student, studying such compounds enhances our understanding of the complex interplay between structure and function in biochemical systems.

Quote from Research

Researchers emphasize that “the intricacies of amino acid derivatives showcase the elegance of biochemical architecture and its influence on biological behavior.”

Overall, this compound exemplifies the intricate nature of amino acids and their derivatives, inviting further exploration into its properties and potential uses.

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