L-Cysteine boronic acid
- Molecular formula
- C5H12BNO4S
- CAS Number
- 89463-19-8
- IUPAC Name
- 2-amino-3-(2-boronoethylsulfanyl)propanoic acid
- Molecular Weight
- 178.01g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5200g/cm3
- Appearance
- is due to its crystalline structure, and it may appear slightly off-white depending on particle size and purity. This appearance is common to many amino acid derivatives, which exhibit similar visual characteristics.
- Synonyms
- 88642-86-8
Identification
Interesting Facts about 2-Amino-3-(2-boronoethylsulfanyl)propanoic Acid
2-Amino-3-(2-boronoethylsulfanyl)propanoic acid, often referred to in the scientific community for its unique properties, is a compound that has garnered attention due to its intriguing structural features and potential applications in various fields. Here are some compelling aspects of this compound:
- Construction of the Molecule: This compound contains both a boron atom and a sulfur atom, which imparts unique chemical reactivity and potential for catalytic activity. The presence of these elements indicates its role in organoboron chemistry, a field that explores the reactivity and synthesis of boron-containing compounds.
- Biological Relevance: Compounds like this one are often studied for their biological implications. For instance, its structure can mimic amino acids, potentially interacting with biological macromolecules, which opens doors for research in pharmacology and biochemical pathways.
- Applications in Drug Design: With the increasing interest in drug design, this compound could be evaluated for its ability to act as a boron-containing biomolecule. Boron compounds are known for their ability to improve the efficacy of drugs and may play a role in targeted therapy.
- Synthesis Techniques: The synthesis of 2-amino-3-(2-boronoethylsulfanyl)propanoic acid can serve as a gateway for students and scientists to explore various organic synthesis methods, especially those involving boron and sulfur chemistry, making it an excellent subject for learning about functional group transformations.
- Research Potential: Ongoing studies into the properties of compounds featuring boron highlight their importance in materials science, catalysis, and medicinal chemistry. This compound can thus serve as a practical example in understanding the bridging between different branches of chemistry.
In conclusion, 2-amino-3-(2-boronoethylsulfanyl)propanoic acid is more than just a chemical formula; it represents a blend of organic chemistry, potential therapeutic applications, and an opportunity for innovative research in modern science. As we delve deeper into its properties and interactions, the possibilities for this compound seem promising!