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NIBOCH (common name)

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Identification
Molecular formula
C18H8Cl6N3
CAS number
1893-26-5
IUPAC name
2-(2-naphthyl)-4,6-bis(trichloromethyl)-1,3,5-triazine
State
State

At room temperature, 2-(2-naphthyl)-4,6-bis(trichloromethyl)-1,3,5-triazine is a solid, often provided as a crystalline powder. It is stable under normal temperatures and pressures.

Melting point (Celsius)
250.00
Melting point (Kelvin)
523.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
451.48g/mol
Molar mass
451.4700g/mol
Density
1.8900g/cm3
Appearence

Appearance: This compound is typically a pale yellow powder. The solid form may vary slightly in color depending on the purity and the specific preparation method used.

Comment on solubility

Solubility of 2-(2-naphthyl)-4,6-bis(trichloromethyl)-1,3,5-triazine

The solubility of 2-(2-naphthyl)-4,6-bis(trichloromethyl)-1,3,5-triazine can be described as quite limited. This compound is known to have low solubility in water, which is characteristic of many chlorinated organic compounds due to their hydrophobic nature. Instead, its solubility is more favorable in organic solvents.

Factors Influencing Solubility:

  • Hydrophobic Character: The presence of trichloromethyl groups contributes to a nonpolar character, reducing interaction with polar solvents like water.
  • Organic Solvent Compatibility: The triazine structure and naphthyl rings provide a better solubility in organic solvents such as acetone, ethanol, or chloroform.
  • Temperature Effects: Typically, warming the solvent can increase solubility, allowing for better dispersion of the compound.

In conclusion, when considering this compound’s solubility, it's important to remember that its performance and application will largely depend on the choice of solvent. As a general guideline, always opt for non-polar to moderately polar solvents for optimal results.

Interesting facts

Interesting Facts about 2-(2-naphthyl)-4,6-bis(trichloromethyl)-1,3,5-triazine

2-(2-naphthyl)-4,6-bis(trichloromethyl)-1,3,5-triazine is a fascinating compound that draws significant interest due to its unique structure and multiple applications in various fields. Here are some intriguing points to consider:

  • Structural Complexity: The compound features a triazine ring, which is known for its stability and versatile reactivity. The substitution with trichloromethyl groups significantly enhances its electrophilic character.
  • Applications in Agriculture: This compound often finds its place as a herbicide, effectively controlling weed populations due to its ability to disrupt photosynthesis in plants.
  • Fluorescent Properties: It has been noted for its fluorescent properties, making it useful in the development of light-emitting materials and fluorescence-based sensors.
  • Research Importance: As a subject of research in organic chemistry, it serves as a model for studying heterocyclic compounds and helps in the development of new chemical methodologies.
  • Environmental Considerations: Given its chlorinated structure, it raises important discussions regarding its environmental impact and the need for careful usage and disposal.

To quote an esteemed scientist in the field, "The versatility of 1,3,5-triazines in synthetic organic chemistry cannot be overstated." This emphasizes the importance of compounds like 2-(2-naphthyl)-4,6-bis(trichloromethyl)-1,3,5-triazine in both academic and practical applications.

In summary, this compound embodies a mix of intrigue, utility, and a vital role in ongoing chemical research. Its unique properties make it an ideal candidate for innovations in agricultural chemistry, materials science, and beyond.

Synonyms
SCHEMBL217194
SCHEMBL9873824
SCHEMBL29389195