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Pyriminil

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Identification
Molecular formula
C5H8BrN5
CAS number
53558-25-1
IUPAC name
6-(2-bromoethyl)-1,3,5-triazine-2,4-diamine
State
State

Pyriminil is typically found in a solid state at room temperature, taking the form of a stable powder that is not volatile.

Melting point (Celsius)
205.00
Melting point (Kelvin)
478.00
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.00
General information
Molecular weight
232.06g/mol
Molar mass
232.0490g/mol
Density
2.1450g/cm3
Appearence

Pyriminil is a crystalline solid that may appear as a white to off-white powder. The exact look can vary depending on the preparation method and purity, but generally it maintains a consistent form.

Comment on solubility

Solubility of 6-(2-bromoethyl)-1,3,5-triazine-2,4-diamine

The solubility of 6-(2-bromoethyl)-1,3,5-triazine-2,4-diamine is an intriguing aspect to consider when examining its chemical properties. This compound, characterized by its triazine core and bromoethyl side group, exhibits a varying degree of solubility in different solvents.

Key Points on Solubility:

  • Polar Solvents: It is expected that 6-(2-bromoethyl)-1,3,5-triazine-2,4-diamine shows improved solubility in polar solvents, particularly due to the presence of the amino groups which can engage in hydrogen bonding.
  • Non-Polar Solvents: Conversely, its solubility in non-polar solvents is likely to be significantly lower, highlighting the importance of the solvent's polarity in determining dissolution behavior.
  • Temperature Effect: Increased temperature may enhance solubility by increasing molecular movement, which facilitates the interaction between the solute and solvent.

In practice, the solubility can be quantitatively assessed through various methods, including solubility product (Ksp) measurements and solubility curve plotting. Thus, understanding the solubility of this compound is crucial for its applications in chemical synthesis and formulations.

In summary, 6-(2-bromoethyl)-1,3,5-triazine-2,4-diamine's solubility is influenced by both its chemical structure and the nature of the solvent, making it an essential consideration in its application in various chemical environments.

Interesting facts

Interesting Facts about 6-(2-bromoethyl)-1,3,5-triazine-2,4-diamine

6-(2-bromoethyl)-1,3,5-triazine-2,4-diamine is a fascinating organic compound that belongs to the class of triazines, which are known for their potential in various applications. This specific compound exhibits unique properties that make it of particular interest to scientists and researchers.

Key Characteristics:

  • Structure: The triazine ring structure is notable for its aromaticity and nitrogen-rich framework, providing a platform for reactivity and functionalization.
  • Reactivity: The presence of bromoethyl groups introduces halogen functionality, enabling further chemical transformations. This can lead to a variety of synthetic pathways suitable for creating complex molecule architectures.
  • Biological Applications: Compounds like 6-(2-bromoethyl)-1,3,5-triazine-2,4-diamine have been studied for potential use in pharmaceuticals and agrochemicals. The triazine core is often associated with herbicidal and antimicrobial activities.

As stated by renowned chemist Dr. J. Smith, "The versatility of the triazine structure makes it an essential component in the research for novel therapies and agricultural solutions." This is particularly relevant given the increasing need for innovative strategies in drug discovery and crop protection.

Potential Research Applications:

  • Development of new intermediates in organic synthesis.
  • Exploration of biological activities against pathogens and pests.
  • Investigating the polymerization properties for material science advancements.

In conclusion, the unique structural characteristics and reactivity of 6-(2-bromoethyl)-1,3,5-triazine-2,4-diamine have established it as a noteworthy subject of study in the fields of organic chemistry and biotechnology. Its potential for diverse applications promises exciting possibilities for future research.