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

Identification

Molecular formula

C₃₃H₂₁N₃O₃

CAS number

56803-37-3

IUPAC name

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

State

At room temperature, 2,4,6-tris(1-naphthyloxy)-1,3,5-triazine is a solid. It maintains its solid form under standard atmospheric conditions, making it suitable for various applications in both industrial and scientific research settings.

Melting point (Celsius)

241.00

Melting point (Kelvin)

514.15

Boiling point (Celsius)

499.00

Boiling point (Kelvin)

772.15

General information

Molecular weight

479.54g/mol

Molar mass

479.5180g/mol

Density

1.3200g/cm³

Appearence

2,4,6-tris(1-naphthyloxy)-1,3,5-triazine typically appears as a pale yellow powder or crystalline solid. The compound is known for its aesthetic solid-state, often possessing a fibrous or powdery texture depending on the method of preparation and processing.

Comment on solubility

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

The solubility of 2,4,6-tris(1-naphthyloxy)-1,3,5-triazine in various solvents can be intriguing. This compound, characterized by its unique structure, exhibits different solubility traits based on its molecular interactions with the solvent medium. Here are some key points to consider:

Polarity: 2,4,6-tris(1-naphthyloxy)-1,3,5-triazine tends to be non-polar due to the presence of naphthyl groups which contribute to hydrophobic interactions.
Solvent Compatibility: It is generally more soluble in organic solvents such as chloroform, dichloromethane, and acetone, while showing low solubility in polar solvents like water.
Temperature Effects: Increased temperatures can enhance the solubility of this compound in organic solvents, encouraging increased molecular motion and overcoming intermolecular forces.
Use in Applications: Understanding its solubility is crucial for its applications in various fields, including material science and organic synthesis, where the solvent choice can affect reaction outcomes.

To summarize, the solubility of 2,4,6-tris(1-naphthyloxy)-1,3,5-triazine is notably influenced by the nature of the solvent and the temperature. It emphasizes the adage, "like dissolves like," highlighting the importance of solvent polarity in the dissolution process.

Interesting facts

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

2,4,6-tris(1-naphthyloxy)-1,3,5-triazine is a fascinating compound with a variety of intriguing properties and applications. Here are some noteworthy aspects:

Structural Significance: This compound features a triazine ring, which is a six-membered aromatic system containing three nitrogen atoms. The triazine moiety is known for its ability to form stable complexes with metals, enhancing its utility in coordination chemistry.
Substituent Influence: The presence of three 1-naphthyloxy groups significantly alters the compound's chemical behavior. Naphthalene derivatives are well-recognized for their electronic properties, making this compound a potential candidate for various organic electronic applications.
Potential Applications: Due to its unique structure and resulting properties, 2,4,6-tris(1-naphthyloxy)-1,3,5-triazine has potential applications in:
- Organic photovoltaics
- Copper corrosion inhibitors
- Antimicrobial agents
Research Interest: Owing to its varied functionalities, this compound is of great interest in research fields such as medicinal chemistry, materials science, and agrochemicals. It exemplifies how specific substitutions can lead to enhanced biological and chemical properties.

Moreover, the intriguing interplay between its structural elements and versatility in application opens doors to numerous experimental studies and potential innovations in synthetic chemistry.

As noted by a prominent chemist, “The beauty of chemistry lies in the connections we make between structure and function.” This compound clearly illustrates that concept, with its robust architecture facilitating diverse practical uses.

Synonyms

SCHEMBL9858926