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1,3,5-Trichloro-2,4,6-triphenylborazine

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Identification
Molecular formula
C18H15B3Cl3N3
CAS number
930-71-0
IUPAC name
1,3,5-trichloro-2,4,6-triphenyl-1,3,5,2,4,6-triazatriborinane
State
State

This compound is a crystalline solid at room temperature, typically exhibiting stability and handling ease under standard conditions.

Melting point (Celsius)
246.00
Melting point (Kelvin)
519.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
393.24g/mol
Molar mass
393.2400g/mol
Density
1.2600g/cm3
Appearence

1,3,5-Trichloro-2,4,6-triphenylborazine is typically seen as a white crystalline solid. The appearance can vary slightly depending on sample purity and handling.

Comment on solubility

Solubility of 1,3,5-trichloro-2,4,6-triphenyl-1,3,5,2,4,6-triazatriborinane

The solubility of 1,3,5-trichloro-2,4,6-triphenyl-1,3,5,2,4,6-triazatriborinane can be quite complex due to its unique structure and functional groups. Here are some key points regarding its solubility behavior:

  • Polarity: The presence of chlorinated groups enhances the compound's polarity, which often favors solubility in polar solvents.
  • Hydrophobic interactions: On the other hand, the triphenyl moieties contribute to the hydrophobic character of the molecule, which can lead to limited solubility in water.
  • Solvent Preference: Typically, compounds of this nature demonstrate better solubility in organic solvents such as chloroform, ethanol, or benzene.
  • Temperature Effects: Like many organic compounds, solubility may increase with temperature due to enhanced molecular motion and interaction with solvents.

As a general guideline, one might say, "A compound’s solubility in a particular solvent reflects its structural affinity for that solvent." Therefore, while 1,3,5-trichloro-2,4,6-triphenyl-1,3,5,2,4,6-triazatriborinane may have specific solubility characteristics, actual assessments should ideally be conducted experimentally to confirm these behaviors across various conditions.

Interesting facts

Interesting Facts about 1,3,5-Trichloro-2,4,6-triphenyl-1,3,5,2,4,6-triazatriborinane

This fascinating compound, known as a triazatriborinane, exhibits a unique chemical structure that makes it stand out in the world of organoboron chemistry. Here are some noteworthy highlights:

  • Complex Structure: The compound features a remarkable arrangement of nitrogen and boron atoms, which contributes to its stability and reactivity in various chemical reactions.
  • Dual Role: Triazatriborinanes can act both as Lewis acids and nucleophiles, making them versatile players in organic synthesis.
  • Applications in Catalysis: This compound has shown potential in catalyzing various chemical reactions, opening doors to new pathways in synthesizing complex organic molecules.
  • Environmental Considerations: Compounds containing chlorine, such as 1,3,5-trichloro derivatives, prompt discussions about environmental impact, particularly regarding their persistence and bioaccumulation in ecosystems.
  • Research Frontier: Scientists are actively exploring the properties of triazatriborinanes, including their applications in materials science and pharmaceuticals, due to their intriguing electronic properties.

The juxtaposition of boron, nitrogen, and chlorine within the compound leads to unique reactivity patterns that continue to engage the scientific community's interest. As researchers delve deeper into its potential, the compound could very well play a critical role in future advancements in synthetic and medicinal chemistry.

Synonyms
BRN 2188485
BORAZINE, 2,4,6-TRICHLORO-1,3,5-TRIPHENYL-
DTXSID90243444
4-12-00-01098 (Beilstein Handbook Reference)
DTXCID90165935