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N-(3,4-dichlorophenyl)-4,6-dimethoxy-1,3,5-triazin-2-amine

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Identification
Molecular formula
C11H11Cl2N3O2
CAS number
4963-87-9
IUPAC name
N-(3,4-dichlorophenyl)-4,6-dimethoxy-1,3,5-triazin-2-amine
State
State
At room temperature, this compound is a solid. It is typically stored at room temperature in a stable environment to maintain its solid state.
Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
327.00
Boiling point (Kelvin)
600.15
General information
Molecular weight
303.12g/mol
Molar mass
303.1240g/mol
Density
1.4600g/cm3
Appearence

N-(3,4-dichlorophenyl)-4,6-dimethoxy-1,3,5-triazin-2-amine is typically a pale yellow crystalline powder. It can appear as finely divided crystals, reflecting its aromatic and heterocyclic structure, which contributes to its crystalline nature.

Comment on solubility

Solubility of N-(3,4-dichlorophenyl)-4,6-dimethoxy-1,3,5-triazin-2-amine

The solubility of N-(3,4-dichlorophenyl)-4,6-dimethoxy-1,3,5-triazin-2-amine can be influenced by various factors, including its molecular structure and the presence of functional groups. Here are some key considerations regarding its solubility:

  • Polarity: The presence of multiple methoxy groups enhances the polarity of the compound, which can aid in solubility in polar solvents.
  • Solvent Compatibility: The compound is likely to be more soluble in organic solvents such as dichloromethane or ethanol, rather than in water due to its hydrophobic character.
  • Temperature Effects: As with many compounds, increased temperature may improve solubility, allowing for better dissolution in chosen solvents.
  • Functional Groups: The –OCH3 groups tend to increase solubility in organic solvents, while the –Cl substituents may affect reactivity rather than solubility.

Overall, understanding the solubility of this compound is essential for applications in synthesis and analysis, as it drives the choice of solvents for various procedures. As emphasized in the study of solubility:

"Solubility is not just about how much can dissolve; it’s about the interactions that dictate behavior in solution."

The behavior of N-(3,4-dichlorophenyl)-4,6-dimethoxy-1,3,5-triazin-2-amine in various solvents provides critical insights for its practical uses in chemical applications.

Interesting facts

N-(3,4-Dichlorophenyl)-4,6-dimethoxy-1,3,5-triazin-2-amine

N-(3,4-Dichlorophenyl)-4,6-dimethoxy-1,3,5-triazin-2-amine, a compound with intriguing applications and properties, belongs to a class of chemicals known as triazenes. Here are some interesting facts about this complex molecule:

  • Chemical Structure: This compound features a triazine ring, which is a six-membered aromatic heterocycle characterized by the presence of three nitrogen atoms. The substitution pattern in this molecule allows it to exhibit unique chemical behavior.
  • Biological Activity: Compounds related to this triazine may show significant biological activity, making them of interest in pharmaceutical research. Studies have suggested that similar derivatives can act as potent antimicrobial agents.
  • Agricultural Use: Certain triazine compounds are widely used in agriculture as herbicides. They are effective in controlling a variety of broadleaf weeds, and understanding their chemical structure can help in optimizing their use and reducing environmental impact.
  • Environmental Considerations: The persistence of triazine compounds in the environment raises concerns, particularly regarding their potential effects on aquatic ecosystems. It is crucial for scientists to balance their agricultural benefits with ecological safety.
  • Synthesis: The synthesis of triazine compounds often involves multi-step reactions, including condensation and cyclization processes. These synthetic pathways are a rich field of study for chemists, driving innovation in organic chemistry.

Understanding compounds like N-(3,4-Dichlorophenyl)-4,6-dimethoxy-1,3,5-triazin-2-amine allows scientists to explore not only their practical applications but also their potential in advancing chemical research and environmental sustainability.