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2-(4-nitrophenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine

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Identification
Molecular formula
C12H3Cl6N4O2S
CAS number
92046-92-5
IUPAC name
2-(4-nitrophenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine
State
State

At room temperature, this compound is typically a solid.

Melting point (Celsius)
173.00
Melting point (Kelvin)
446.15
Boiling point (Celsius)
396.00
Boiling point (Kelvin)
669.15
General information
Molecular weight
437.54g/mol
Molar mass
437.5420g/mol
Density
1.6100g/cm3
Appearence

The compound typically appears as a crystalline solid, often in a pale yellow color.

Comment on solubility

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

The solubility of 2-(4-nitrophenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine is influenced by several key factors:

  • Polarity: The presence of both the nitrophenyl and trichloromethyl groups indicates a complex structure, which may contribute to its polarity and affect solubility in various solvents.
  • Solvent Interactions: This compound may be more soluble in organic solvents such as acetone or ethyl acetate rather than in polar solvents like water.
  • Hydrophobic vs. Hydrophilic: The trichloromethyl groups are usually hydrophobic, suggesting that the compound may exhibit limited solubility in aqueous environments.

Overall, due to the intricate balance of hydrophobic and hydrophilic characteristics within its molecular structure, one can anticipate that the solubility of this compound is relatively low in water, while it may find better solubility in non-polar organic solvents.

As a general rule, remember that "like dissolves like," which emphasizes the importance of matching solvent types to the chemical nature of the solute. Thus, successful solubilization will depend on choosing the right solvent to harness the unique properties of 2-(4-nitrophenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine.

Interesting facts

Interesting Facts About 2-(4-nitrophenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine

2-(4-nitrophenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine is a fascinating compound that plays a significant role in various chemical applications. Here are some key points that make this compound particularly interesting:

  • Unique Structure: The compound features a triazine ring, known for its stability and ability to participate in various chemical reactions. The incorporation of both nitro and trichloromethyl groups adds to its reactivity and versatility.
  • Applications: This compound is often utilized as a building block in the synthesis of agrochemicals, pharmaceuticals, and materials science. Its properties allow for the development of effective herbicides and insecticides.
  • Reactivity: Due to the presence of the trichloromethyl groups, this compound demonstrates considerable electrophilic character, making it an attractive target for nucleophilic substitution reactions.
  • Environmental Impact: Compounds like this are studied for their environmental fate and transport, as the trichloromethyl groups can lead to persistent organic pollutants in ecological systems.
  • Research Potential: Recent studies have investigated derivatives of this compound, leading to potential enhancements in bioactivity and selectivity, which could pave the way for safer agricultural practices.

In summary, 2-(4-nitrophenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine is more than just a chemical entity; it embodies the interplay of structure and function that is essential for innovation in chemical synthesis and practical applications. As stated by a prominent chemist, "The beauty of chemistry lies in its ability to transform and adapt." This compound certainly exemplifies that notion.

Synonyms
2-(4-nitrophenyl)sulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine
24478-14-6
DTXSID10274952