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2-Methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine

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Identification
Molecular formula
C10H13Cl3N4
CAS number
940-44-9
IUPAC name
2-methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine
State
State

At room temperature, this compound is a solid. It is often encountered in the form of crystalline powder.

Melting point (Celsius)
68.00
Melting point (Kelvin)
341.15
Boiling point (Celsius)
346.70
Boiling point (Kelvin)
619.85
General information
Molecular weight
273.66g/mol
Molar mass
273.6550g/mol
Density
1.4620g/cm3
Appearence

2-Methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine appears as a crystalline solid. The crystals are typically white to off-white in color.

Comment on solubility

Solubility of 2-methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine

The solubility of 2-methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine is an important aspect to consider for its applications and behaviors in various environments. This compound is characterized by its complex structure, and its solubility can be influenced by several factors:

  • Polarity: The presence of multiple functional groups, including the trichloromethyl group, may enhance its polarity, affecting its interaction with solvents.
  • Solvent Type: It typically exhibits better solubility in polar solvents such as dimethyl sulfoxide (DMSO) and dimethylformamide (DMF), while being less soluble in non-polar solvents.
  • Temperature Dependency: Like many compounds, its solubility may increase with temperature, making it more soluble in hotter conditions.
  • pH Influence: The solubility can also vary with the pH of the solution, especially due to the piperidyl component which can exist in different ionic forms.

In general, the solubility of 2-methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine underscores the necessity of carefully selecting appropriate solvents for practical applications. Understanding these solubility characteristics is crucial for optimizing its use in scientific and industrial contexts.

Interesting facts

Exploring 2-methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine

2-Methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine, often referred to in the context of agrochemicals and medicinal chemistry, exhibits a fascinating combination of properties that capture the interest of both researchers and students alike. This compound belongs to the triazine family, which is known for its diverse applications due to the presence of nitrogen atoms that contribute to its unique reactivity.

Key Features of 2-methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine:

  • Agricultural Applications: This compound is significant in the agricultural sector as it is used as a herbicide. Its ability to inhibit photosynthesis pathways makes it effective in controlling unwanted plant growth.
  • Structural Complexity: The inclusion of a piperidine ring enhances its biological activity. Piperidine is a common motif in many pharmaceuticals, enabling the compound to interact with biological targets effectively.
  • Halogenated Characteristics: The presence of trichloromethyl groups equips the compound with high reactivity and lipophilicity, which are favorable for various chemical reactions in both synthetic and biological contexts.
  • Research Potential: Due to its structural attributes, this triazine derivative is a subject of ongoing research, particularly in understanding its mechanism of action and developing novel derivatives that may improve efficacy and reduce environmental impact.

As one delves into the chemistry of 2-methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine, one is reminded of the words of renowned chemist Linus Pauling, who stated, "The best way to have a good idea is to have a lot of ideas." This compound is a testament to the myriad of ideas that chemistry can inspire, leading to innovations in agriculture and beyond.

In conclusion, 2-methyl-4-(1-piperidyl)-6-(trichloromethyl)-1,3,5-triazine not only provides fascinating insights into organic synthesis and pesticide development but also encourages inquiry into broader chemical principles and their impact on the world.