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2-(allylamino)-4-allyloxy-6-(diazonioamino)-1,3,5-triazine

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Identification
Molecular formula
C9H12N6O
CAS number
69425-87-8
IUPAC name
2-(allylamino)-4-allyloxy-6-(diazonioamino)-1,3,5-triazine
State
State

The compound is typically a solid at room temperature, exhibiting a crystalline structure. It needs to be stored in dry conditions to maintain its stability.

Melting point (Celsius)
122.00
Melting point (Kelvin)
395.15
Boiling point (Celsius)
540.00
Boiling point (Kelvin)
813.15
General information
Molecular weight
252.26g/mol
Molar mass
252.2640g/mol
Density
1.3618g/cm3
Appearence

The compound appears as a crystalline solid, which may range in color from white to pale yellow depending on purity and environmental conditions.

Comment on solubility

Solubility of 2-(allylamino)-4-allyloxy-6-(diazonioamino)-1,3,5-triazine

When discussing the solubility of the compound 2-(allylamino)-4-allyloxy-6-(diazonioamino)-1,3,5-triazine, several factors come into play:

  • Polarity: Given its structure, this compound exhibits a range of polar functional groups that can enhance solubility in polar solvents.
  • pH Sensitivity: The presence of the diazonium group may lead to variable solubility in different pH environments, as the protonation state can significantly alter solubilizing behaviors.
  • Solvent Compatibility: It is expected to have better solubility in organic solvents, such as ethanol or dimethyl sulfoxide (DMSO), due to the hydrophobic allyl groups.

To sum up, this compound likely displays:

  1. Increased solubility in polar solvents due to its functional groups.
  2. Potentially variable solubility based on the pH of the surrounding environment.

Overall, one could say: “The solubility of 2-(allylamino)-4-allyloxy-6-(diazonioamino)-1,3,5-triazine is influenced by its complex structure and environmental conditions.”

Interesting facts

Interesting Facts about 2-(allylamino)-4-allyloxy-6-(diazonioamino)-1,3,5-triazine

2-(allylamino)-4-allyloxy-6-(diazonioamino)-1,3,5-triazine is a fascinating compound that showcases the versatility of organic chemistry, particularly in the realm of heterocyclic compounds. This compound belongs to the triazine family, which is known for its unique six-membered ring structure containing nitrogen atoms.

Here are some intriguing aspects of this compound:

  • Functional Diversity: The presence of both allylamino and allyloxy groups contributes to its interesting chemical reactivity. These functional groups allow for various modifications and applications in different fields.
  • Role in Dye Chemistry: Compounds like this one can serve as intermediates in dye synthesis. The diazonium group enhances the potential for reactivity, making it a valuable tool in the production of azo dyes.
  • Biological Activity: Research indicates that triazine derivatives possess a wide range of biological activities, including antimicrobial, antiviral, and herbicidal properties. This makes them significant in pharmaceuticals and agricultural applications.
  • Dyes and Pigments: The incorporation of diazonium functionalities is crucial in synthesizing vivid dyes and pigments, which are essential in textiles and plastics. It opens up avenues for creating colorful materials.

As scientists continue to explore the potential applications of 2-(allylamino)-4-allyloxy-6-(diazonioamino)-1,3,5-triazine, they uncover its significance in sustainable chemistry and innovations in materials science. This compound encourages the scientific community to delve deeper into the effects of chemical structures on reactivity and application.

In summary, the unique structure and functional versatility of 2-(allylamino)-4-allyloxy-6-(diazonioamino)-1,3,5-triazine make it a compound of considerable interest, paving the way for advancements in various chemical industries.