Tris(2-chlorophenyl) borate
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- Molecular formula
- C18H12BCl3O3
- CAS Number
- 29405-33-6
- IUPAC Name
- tris(2-chlorophenyl) borate
- Molecular Weight
- 356.90g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3500g/cm3
- Synonyms
- Tris(2-chlorophenyl) borate
Identification
Interesting facts
Interesting Facts about Tris(2-Chlorophenyl) Borate
Tris(2-chlorophenyl) borate is an intriguing compound known for its multifaceted properties and applications in various fields. Here are some fascinating insights:
- Versatile Applications: This compound is primarily utilized as a reagent in organic synthesis, playing a crucial role in the formation of boron-centered intermediates, which are vital in constructing complex organic molecules.
- Biological Relevance: Tris(2-chlorophenyl) borate has shown potential in biological applications, particularly in the context of membrane-active agents. It's been studied for its effects on cellular membranes, making it a compound of interest in pharmacological research.
- Structure and Stability: The presence of chlorophenyl groups enhances the compound's stability and reactivity, which is essential for its performance in various reactions.
- Environmental Impact: Understanding the environmental behavior of this compound is critical, as it may contribute to ecological toxicity studies. Awareness of how such compounds interact with the environment is increasingly vital in chemical research.
- Historical Relevance: Tris(2-chlorophenyl) borate has been referenced in various scientific literature since the late 20th century, reflecting the evolving understanding of boron chemistry and its significance in organic and medicinal chemistry.
As researchers continue to delve deeper into the characteristics and applications of tris(2-chlorophenyl) borate, it remains a compelling subject for those interested in the intersection of organic synthesis and biological activity. Its unique properties highlight the importance of boron-containing compounds in modern chemistry.