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Tris(2-chlorophenyl) borate

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Identification
Molecular formula
C18H12BCl3O3
CAS number
29405-33-6
IUPAC name
tris(2-chlorophenyl) borate
State
State

At room temperature, tris(2-chlorophenyl) borate is in a solid state. It is often encountered in powder or crystalline form.

Melting point (Celsius)
148.00
Melting point (Kelvin)
421.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
356.90g/mol
Molar mass
356.9000g/mol
Density
1.3500g/cm3
Appearence

Tris(2-chlorophenyl) borate typically appears as a white to off-white crystalline powder. Its crystalline nature contributes to its solid form at room temperature, and it usually lacks any distinct odor.

Comment on solubility

Solubility of Tris(2-chlorophenyl) borate

Tris(2-chlorophenyl) borate is a fascinating compound with particular solubility characteristics that can affect its application and behavior in various environments. Understanding its solubility is key to utilizing this compound effectively. Here are some important aspects to consider:

  • Solvent Compatibility: It is known to be sparingly soluble in water, which limits its use in aqueous environments. However, it may dissolve more readily in organic solvents, such as:
    • Acetone
    • Chloroform
    • Benzene
  • Temperature Influence: The solubility of tris(2-chlorophenyl) borate can increase with temperature. As the solvent's temperature rises, the kinetic energy of the molecules also increases, enabling greater interaction and dissolution.
  • pH Relevance: The solubility may also be influenced by the pH of the solution. Adjusting the pH can alter the charge distribution and polarity of the compound, potentially enhancing or reducing its solubility.

In conclusion, the solubility of tris(2-chlorophenyl) borate is influenced by various factors, including the choice of solvent, temperature, and pH. It is crucial to consider these elements when planning experiments or applications involving this compound to achieve optimal results.

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.

Synonyms
Tris(2-chlorophenyl) borate
5337-60-0
Tri-o-chlorophenyl borate
Boric acid, tri(o-chlorophenyl) ester
Boric acid, tris(o-chlorophenyl) ester
BORIC ACID, TRI-o-CHLOROPHENYL ESTER
2KGW54P4PP
NSC-808
NSC 808
EINECS 226-263-3
BRN 2546654
starbld0019201
Tri(o-chlorophenyl) borate
UNII-2KGW54P4PP
4-06-00-00810 (Beilstein Handbook Reference)
SCHEMBL738763
NSC808
WLN: GR BOBOR BG&OR BG
DTXSID40201534
JNEZJAAADKQBBD-UHFFFAOYSA-N
Boric acid, tris(2-chlorophenyl) ester
NS00032739