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2,4,6-Tris(4-chlorophenyl)-1,3,5-triazine-2,4,6-triamine

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Identification
Molecular formula
C21H15Cl3N6
CAS number
128-39-2
IUPAC name
N2,N4,N6-tris(4-chlorophenyl)-1,3,5-triazine-2,4,6-triamine
State
State

At room temperature, the compound exists in a solid state. It maintains stability and does not readily sublime or decompose under normal conditions, providing a robust and consistent form for various applications.

Melting point (Celsius)
235.00
Melting point (Kelvin)
508.15
Boiling point (Celsius)
438.20
Boiling point (Kelvin)
711.35
General information
Molecular weight
465.83g/mol
Molar mass
465.8250g/mol
Density
1.4590g/cm3
Appearence

This compound is commonly a pale yellow crystalline solid. The solid is characterized by its well-defined crystal lattices and uniform color, indicative of its purity. The appearance may vary slightly depending on the form in which it's processed or handled.

Comment on solubility

Solubility of N2,N4,N6-tris(4-chlorophenyl)-1,3,5-triazine-2,4,6-triamine

The solubility of N2,N4,N6-tris(4-chlorophenyl)-1,3,5-triazine-2,4,6-triamine is a fascinating topic worth exploring. This compound, characterized by its complex structure, exhibits unique solubility properties that can be affected by various factors:

  • Polarity: Due to the presence of multiple chlorine atoms attached to the aromatic rings, the overall polarity of the compound is enhanced, which generally can lead to solubility in polar solvents.
  • Hydrogen Bonding: The triamine functionality suggests the potential for hydrogen bonding, which may increase solubility in solvents capable of engaging in such interactions.
  • Solvent Type: Solubility in nonpolar solvents tends to be lower, whereas in polar solvents like water or DMSO, the solubility may increase due to enhanced interactions.

Moreover, it is important to note that the solubility of this compound is not extensively documented, making experimental data essential for a comprehensive understanding. As with many organic compounds, the conditions—such as temperature and pH—can dramatically influence solubility. Thus, a careful evaluation of specific solvent interactions is necessary for accurate applications in chemical processes.

Interesting facts

Interesting Facts About N2,N4,N6-tris(4-chlorophenyl)-1,3,5-triazine-2,4,6-triamine

N2,N4,N6-tris(4-chlorophenyl)-1,3,5-triazine-2,4,6-triamine, often referred to in scientific literature as a member of the triazine family, showcases some fascinating characteristics:

  • Versatile Applications: This compound is known for its extensive use in the field of agrochemicals, particularly as a herbicide due to its ability to inhibit certain enzymes in plants.
  • Structural Complexity: The presence of three chlorophenyl groups enhances its chemical stability and multifunctionality, making it an interesting subject for synthetic chemists.
  • Biological Activity: Studies indicate that the compound may exhibit antimicrobial properties, showcasing potential beyond its initial agricultural applications.
  • Environmental Impact: Understanding the degradation pathways of this compound is crucial for assessing its environmental impact and developing strategies for its safe use.

As a chemist or student delving into this compound, one might ponder: “How do substitutions on the triazine ring influence biological activity?” This opens exciting avenues for research into structure-activity relationships in related compounds.

In summary, N2,N4,N6-tris(4-chlorophenyl)-1,3,5-triazine-2,4,6-triamine stands as an exemplary case of how synthetic chemistry can converge with environmental science and agrochemicals, woven into a narrative that continues to unfold as research progresses.

Synonyms
2-N,4-N,6-N-tris(4-chlorophenyl)-1,3,5-triazine-2,4,6-triamine
SCHEMBL11630110
N~2~,N~4~,N~6~-tris(4-chlorophenyl)-1,3,5-triazine-2,4,6-triamine