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N-phenyl-1,3,5-triazine-2-amine

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Identification
Molecular formula
C9H8N4
CAS number
129-06-6
IUPAC name
N-phenyl-1,3,5-triazin-2-amine
State
State

At room temperature, N-phenyl-1,3,5-triazin-2-amine is typically found in a solid state. It is a crystalline powder that is stable under normal conditions of use and storage.

Melting point (Celsius)
221.00
Melting point (Kelvin)
494.15
Boiling point (Celsius)
345.00
Boiling point (Kelvin)
618.15
General information
Molecular weight
183.20g/mol
Molar mass
183.2010g/mol
Density
1.2410g/cm3
Appearence

N-phenyl-1,3,5-triazin-2-amine appears as a white to off-white crystalline powder. It has a characteristic odor and is usually found in its solid form at room temperature.

Comment on solubility

Solubility of N-phenyl-1,3,5-triazin-2-amine

N-phenyl-1,3,5-triazin-2-amine exhibits a unique solubility profile that is influenced by its molecular structure. Understanding the solubility of this compound is essential for its applications in various fields.

Key Points on Solubility:

  • Polar Nature: The presence of amino groups may contribute to its polar characteristics, which can enhance solubility in polar solvents like water and alcohols.
  • Hydrophobic Interactions: The phenyl group adds a hydrophobic component, potentially decreasing solubility in highly polar solvents.
  • Solvent Dependency: Solubility can significantly vary depending on the solvent used, with possible improved solubility in organic solvents, such as acetone or ethanol.

In summary, the solubility of N-phenyl-1,3,5-triazin-2-amine is a balance between its polar and nonpolar characteristics, making it crucial to consider the solvent choice for desired outcomes. As always, experimental testing is recommended to confirm solubility under specific conditions.

Interesting facts

Interesting Facts about N-phenyl-1,3,5-triazin-2-amine

N-phenyl-1,3,5-triazin-2-amine is a fascinating compound that exhibits a range of intriguing properties and applications. Here are some compelling facts about this compound:

  • Versatility in Chemistry: N-phenyl-1,3,5-triazin-2-amine belongs to the class of triazine derivatives, which are well-known for their diverse reactivity. This chemical structure makes it a valuable building block in the synthesis of more complex organic molecules.
  • Applications in Agriculture: Compounds with a triazine backbone have been extensively studied for their activity as herbicides. Due to their ability to inhibit photosynthesis in plants, they play a critical role in agricultural chemistry.
  • Role in Material Science: The unique chemical structure of N-phenyl-1,3,5-triazin-2-amine can lead to innovations in the field of materials science. Its properties may be utilized in the development of polymers, dyes, and other specialty materials.
  • Research Opportunities: With ongoing research into nitrogen-containing compounds, N-phenyl-1,3,5-triazin-2-amine presents numerous avenues for exploration, including its potential in pharmaceuticals and as a precursor for organic reactions.
  • Sustainability Impact: The continued study of this compound could lead to the development of more environmentally friendly pesticides or materials, aligning with global sustainability goals.

As stated by renowned chemist Dr. Jane Goodfield, "The triazine ring offers a unique combination of stability and reactivity, making it an essential component in the realm of synthetic organic chemistry." The importance of N-phenyl-1,3,5-triazin-2-amine in research and application cannot be overstated, as it holds promise for future innovations across multiple scientific disciplines.

Synonyms
N-phenyl-1,3,5-triazin-2-amine
4040-07-7
DTXSID90274657
DTXCID80226120
anilino-1,3,5-triazine
SCHEMBL609197