Interesting facts
Interesting Facts about 6-butyl-N2,N4-diethyl-1,3,5-triazine-2,4-diamine
6-butyl-N2,N4-diethyl-1,3,5-triazine-2,4-diamine, often referred to as a type of triazine derivative, showcases some fascinating chemical characteristics and applications in various fields. Here are some noteworthy points:
- Structural Complexity: The compound is part of the triazine family featuring a unique three-ring structure. This contributes to its diverse reactivity and potential applications.
- Potential Biological Activity: Many triazine derivatives have been studied for anti-cancer, herbicidal, and fungicidal properties, making them significant in agricultural and medicinal chemistry.
- Versatile Functional Groups: With both butyl and diethyl functional groups present, this compound has increased lipophilicity, which may influence its bioavailability and solubility properties, thus broadening its application scope.
- Research Interest: Scientists are currently exploring this compound's potential as a building block in the synthesis of more complex organic molecules. As a result, it often features in theoretical chemistry studies and practical laboratory experiments.
As with many compounds in the triazine family, 6-butyl-N2,N4-diethyl-1,3,5-triazine-2,4-diamine opens the door for a deeper understanding of chemical behavior and application in technology and biology. Its promising properties make it an exciting subject for further research and development.
Synonyms
6-butyl-2-N,4-N-diethyl-1,3,5-triazine-2,4-diamine
26235-27-8
DTXSID70275041
Solubility of 6-butyl-N2,N4-diethyl-1,3,5-triazine-2,4-diamine
The solubility of 6-butyl-N2,N4-diethyl-1,3,5-triazine-2,4-diamine is a subject of interest, particularly due to its potential applications in various fields. Here are some key considerations regarding its solubility:
In summary, while the exact solubility of 6-butyl-N2,N4-diethyl-1,3,5-triazine-2,4-diamine can depend on the medium and conditions, we can speculate that its polar amines may enhance solubility in polar solvents like water, whereas its alkyl groups may favor solubility in organic solvents. Further experimental data would be essential to confirm these predictions.