4,6-Difluoro-N-phenyl-1,3,5-triazin-2-amine

Identification

Molecular formula

C₉H₅F₂N₄

CAS number

4213-86-5

IUPAC name

4,6-difluoro-N-phenyl-1,3,5-triazin-2-amine

State

At room temperature, 4,6-difluoro-N-phenyl-1,3,5-triazin-2-amine is typically a solid. It is stable under standard conditions and does not decompose readily.

Melting point (Celsius)

106.00

Melting point (Kelvin)

379.15

Boiling point (Celsius)

341.00

Boiling point (Kelvin)

614.15

General information

Molecular weight

214.16g/mol

Molar mass

214.1750g/mol

Density

1.4175g/cm³

Appearence

4,6-Difluoro-N-phenyl-1,3,5-triazin-2-amine generally appears as a crystalline solid. It is a white to off-white powder and can have a slight aromatic odor due to its organic structure.

Comment on solubility

Solubility of 4,6-difluoro-N-phenyl-1,3,5-triazin-2-amine

The solubility of 4,6-difluoro-N-phenyl-1,3,5-triazin-2-amine can be quite intriguing, as it showcases the interplay of various factors affecting its dissolution in different solvents. Several aspects contribute to its solubility characteristics:

Polarity: The presence of fluorine atoms in the chemical structure leads to differing polar characteristics compared to more traditional organic compounds.
Hydrogen bonding: The amine group can contribute to potential hydrogen bonding interactions, particularly in polar solvents.
Solvent effects: It's crucial to consider that solubility is solvent-dependent. For instance, 4,6-difluoro-N-phenyl-1,3,5-triazin-2-amine is likely to be more soluble in organic solvents than in water due to its hydrophobic phenyl group.
Temperature sensitivity: Changes in temperature can significantly influence the solubility, often increasing it with higher temperatures.

As a general note, "like dissolves like" is a valuable principle here. Thus, this compound’s solubility will be greatly influenced by its ability to interact with the solvent molecules in terms of polarity and size. Understanding these nuances is key to predicting the behavior of 4,6-difluoro-N-phenyl-1,3,5-triazin-2-amine in various solvent environments.

Interesting facts

Interesting Facts about 4,6-Difluoro-N-phenyl-1,3,5-triazin-2-amine

The compound 4,6-difluoro-N-phenyl-1,3,5-triazin-2-amine is a fascinating member of the triazine family, well-known for its diverse applications in the fields of agriculture and pharmaceuticals. Here are some noteworthy points about this intriguing molecule:

Structure and Stability: The unique triazine ring structure provides remarkable stability to the compound, making it resistant to various environmental factors.
Fluorine Substitution: The presence of fluorine atoms not only enhances the compound's biological activity but also improves lipophilicity, potentially increasing its efficacy in target systems.
Pharmacological Relevance: Compounds containing triazine moieties have shown promise as effective herbicides and fungicides, demonstrating their critical role in crop protection.
Research Potential: The continued study of 4,6-difluoro-N-phenyl-1,3,5-triazin-2-amine can lead to new discoveries in drug design, particularly in targeting specific biological pathways due to its selective action.
Sustainability and Safety: Investigating the environmental impact and biodegradability of this compound is essential as chemists strive to create safer agricultural chemicals to minimize ecological harm.

In conclusion, 4,6-difluoro-N-phenyl-1,3,5-triazin-2-amine represents an exciting avenue for scientific exploration. As chemistry students and professionals delve deeper into its characteristics and potential uses, they may uncover innovative applications that could benefit both human health and the environment.

Synonyms

SCHEMBL9685913