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- Molecular formula
- C9H15N3O2S2
- CAS Number
- 62571-86-2
- IUPAC Name
- 2-amino-3-(N-benzyl-C-sulfanyl-carbonimidoyl)sulfanyl-propanoic acid
- Molecular Weight
- 217.28g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4173g/cm3
Identification
Interesting facts
Interesting Facts about 2-amino-3-(N-benzyl-C-sulfanyl-carbonimidoyl)sulfanyl-propanoic acid
This compound is an intriguing member of the amino acids family, specifically classified as a modified amino acid, with noteworthy properties and potential applications. Here are some engaging facts:
- Unique Structure: The presence of both sulfanyl groups in the molecular structure provides interesting reactivity and bonding possibilities that are not typically found in standard amino acids.
- Pharmacological Research: Given its complex arrangement, this compound has potential implications in medicinal chemistry, especially in the area of drug design where sulfur-containing compounds are gaining attention for their biological activities.
- Versatile Synthesis: The synthesis of this compound often involves various organic reactions, showcasing the versatility of synthetic methodologies in modern organic chemistry. Such reactions can include amide coupling and carbon-sulfur bond formation.
- Biological Relevance: As a derivative of propanoic acid, it may also be explored for its role in metabolic pathways and its interactions with enzymes, offering insights into metabolic engineering.
- Potential Applications: With its unique characteristics, this compound could be relevant in fields such as pharmaceuticals, agrochemicals, and nutraceuticals, especially in the development of innovative therapeutic agents.
In summary, 2-amino-3-(N-benzyl-C-sulfanyl-carbonimidoyl)sulfanyl-propanoic acid presents a fascinating area for research within chemistry and biology. Its structural features and potential applications underscore the richness of the chemical landscape that modern scientists explore.