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2,4,6-tris(p-tolylsulfanyl)-1,3,5-triazine

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Identification
Molecular formula
C24H21N3S3
CAS number
86273-11-8
IUPAC name
2,4,6-tris(p-tolylsulfanyl)-1,3,5-triazine
State
State

At room temperature, it is typically a solid.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
412.00
Boiling point (Kelvin)
685.15
General information
Molecular weight
441.64g/mol
Molar mass
441.6420g/mol
Density
1.3200g/cm3
Appearence

The compound appears as a pale yellow solid or powder, which is largely insoluble in water but soluble in organic solvents.

Comment on solubility

Solubility of 2,4,6-tris(p-tolylsulfanyl)-1,3,5-triazine

The solubility of 2,4,6-tris(p-tolylsulfanyl)-1,3,5-triazine in various solvents offers insight into its chemical behavior and potential applications. Generally, the solubility of this compound can be influenced by several factors:

  • Polarity of the solvent: Non-polar solvents like hexane may dissolve 2,4,6-tris(p-tolylsulfanyl)-1,3,5-triazine better than polar solvents due to its sulfonyl groups.
  • Temperature: Increasing temperature often enhances solubility for many compounds. Testing solubility at different temperatures can reveal optimal conditions.
  • Concentration: Concentration varies significantly; thus, comparing saturated solutions can clarify its solubility limits.

Overall, it is essential to consider that 2,4,6-tris(p-tolylsulfanyl)-1,3,5-triazine is likely more soluble in organic solvents due to the hydrophobic nature of the p-tolyl groups. It is also noteworthy that the presence of sulfonyl groups contributes to its potential interaction with other chemical species, influencing its solubility profile significantly.

Further investigation into its solubility characteristics can provide valuable information for its application in various fields, including materials science and organic synthesis.

Interesting facts

Interesting Facts about 2,4,6-tris(p-tolylsulfanyl)-1,3,5-triazine

2,4,6-tris(p-tolylsulfanyl)-1,3,5-triazine is a fascinating compound within the field of chemistry, known for its unique structure and notable applications:

  • Versatile Chemical Structure: This compound features a triazine ring, which is a planar aromatic system made up of three nitrogen atoms and three carbon atoms. The substitution with p-tolylsulfanyl groups enhances its chemical reactivity and solubility in organic solvents.
  • Applications: Due to its distinctive properties, this compound can serve as a valuable intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of specialty chemicals and dyes.
  • Insights into Aromatic Chemistry: The inclusion of p-tolylsulfanyl groups on the triazine core contributes to the compound's electron-donating character, influencing reactions such as nucleophilic substitutions and electrophilic aromatic substitutions.
  • Potential in Material Science: Researchers are investigating compounds like 2,4,6-tris(p-tolylsulfanyl)-1,3,5-triazine for their potential in creating advanced materials, including polymers and nanocomposites, due to their tunable properties.

As a researcher or a student in chemistry, delving into the world of heterocycles like this compound opens up a treasure trove of exciting possibilities in both fundamental and applied science. Each new discovery leads to an improved understanding of how such compounds behave in various chemical reactions and their potential to solve real-world problems.

Synonyms
2,4,6-Tris(p-tolylthio)-1,3,5-triazine
SCHEMBL13752159