Thioglycolylglycine

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Identification

Molecular formula
C4H7NO3S
CAS Number
929-53-9
IUPAC Name
2-(2-amino-2-oxo-ethyl)sulfanylacetamide
Molecular Weight
149.19g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4450g/cm3
Synonyms
14618-65-6
Interesting facts

Interesting Facts about 2-(2-amino-2-oxo-ethyl)sulfanylacetamide

2-(2-amino-2-oxo-ethyl)sulfanylacetamide, often referred to as a derivative in the realm of organic compounds, exhibits fascinating characteristics that make it an intriguing subject for both chemists and students alike. Here are some notable points:

  • Biological Relevance: This compound plays a role in biological systems, potentially serving as a precursor to important biochemical pathways, which may contribute to therapeutic activities.
  • Functional Group Diversity: The presence of multiple functional groups, such as the amine, carbonyl, and sulfanyl groups, offers insight into various chemical reactivity patterns, expanding the potential applications in medicinal chemistry.
  • Synthesis Versatility: Synthetic pathways to create this compound often involve innovative reactions, showcasing the versatility of organic synthesis techniques, which can serve as a learning experience for aspiring chemists.
  • Analytical Techniques: Characterization of this compound often requires the use of sophisticated analytical methods such as NMR spectroscopy and mass spectrometry, which help in understanding its structure and properties better.
  • Potential Applications: Given its structural complexity, it holds promise for various applications in pharmaceuticals, including potential roles as a drug candidate or a biochemical probe.

In summary, 2-(2-amino-2-oxo-ethyl)sulfanylacetamide stands out not only for its chemical properties but also for its implications in real-world chemistry. As chemistry continues to evolve, compounds like this one remind us of the intricate relationships between molecular structure and function.

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