Interesting facts
Interesting Facts about 2-Ethylsulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine
2-Ethylsulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine is a fascinating compound that showcases the intricate connection between chemistry and practical applications.
Key Characteristics
- Structural Complexity: This compound features a triazine ring, which is known for its ability to stabilize various functional groups, making it an essential component in diverse chemical reactions.
- Biological Relevance: Compounds like this one can exhibit herbicidal properties, which make them valuable in agricultural chemistry. Their potency can help manage weed populations effectively.
- Halogen Influence: The presence of trichloromethyl groups is significant, as halogen atoms enhance reactivity and bioactivity, often leading to increased efficacy in herbicide formulations.
- Synthetic Utility: The unique structural features of this triazine derivative allow it to be synthesized or modified easily, providing a platform for the design of new compounds with tailored functionalities.
Applications in Chemistry
Due to its unique properties, this compound can serve as a case study in various fields:
- Pharmaceuticals: Exploring potential biochemical pathways where this compound could play a role in drug discovery or development.
- Materials Science: Investigating the use of similar structures in creating novel materials with specific properties, such as improved stability or resistant to degradation.
- Environmental Science: Studying the environmental impact of such compounds and their persistence in ecosystems can inform safety practices and regulatory measures.
In summary, 2-ethylsulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine demonstrates the synthetic versatility and practical importance of triazine derivatives within the chemical landscape. Scientists continue to explore its potential applications, highlighting the importance of understanding such compounds in developing innovative solutions in chemistry and related disciplines.
Synonyms
s-Triazine, 2-(ethylthio)-4,6-bis(trichloromethyl)-
SCHEMBL11338412
1,3,5-Triazine, 2-(ethylthio)-4,6-bis(trichloromethyl)-
GXCJDHJIPHAPGL-UHFFFAOYSA-N
2-(Ethylsulfanyl)-4,6-bis(trichloromethyl)-1,3,5-triazine #
Solubility of 2-ethylsulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine
The solubility of 2-ethylsulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine presents unique characteristics influenced by its chemical structure. This compound exhibits limited solubility in water, a typical trait for many chlorinated organic molecules. The presence of trichloromethyl groups contributes to hydrophobic interactions, making the compound less favorable for dissolution in polar solvents.
Key points about its solubility include:
In summary, the solubility characteristics of 2-ethylsulfanyl-4,6-bis(trichloromethyl)-1,3,5-triazine are primarily dictated by its chlorinated functional groups, which favor solubility in non-polar or weakly polar organic solvents rather than in aqueous environments. Care must be taken when handling this compound, considering its solubility implications for application and environmental impact.