Interesting facts
Interesting Facts about 1,3,4,6-Tetrachlorocyclohexa-1,4-diene
1,3,4,6-Tetrachlorocyclohexa-1,4-diene is a fascinating chemical compound that embodies the intricate world of organic chemistry. Below are some compelling insights into this unique compound:
- Chlorinated Compound: With four chlorine atoms attached to its cyclohexadiene framework, this compound showcases the remarkable study of chlorination, which is often utilized in various industrial applications.
- Stability and Reactivity: The presence of double bonds in its structure hints at a delicate balance between stability and reactivity. Chemists often explore such structures to understand how they undergo reactions, especially in the context of electrophilic addition reactions due to the electron-withdrawing effect of the chlorines.
- Applications: Chlorinated compounds like this one are often used in pesticides, herbicides, and pharmaceuticals. They serve as pivotal intermediates in synthetic pathways, introducing vital functional groups to the molecules.
- Environmental Impact: The ecological footprint of chlorinated compounds has led to extensive research focusing on their biodegradation and impact on ecosystems, making this compound a topic of environmental chemistry discussions.
- Synthetic Pathways: The synthesis of 1,3,4,6-tetrachlorocyclohexa-1,4-diene can be a topic of study to introduce students to reaction mechanisms and synthetic strategies in organic chemistry.
In summary, 1,3,4,6-tetrachlorocyclohexa-1,4-diene is a compound that not only offers insights into molecular structure and reactivity but also plays a significant role in both industrial applications and environmental chemistry discussions. As one researcher aptly put it, “Every molecule tells a story; it's our job to understand its narrative.”
Synonyms
1,3,4,6-tetrachloro-1,4-cyclohexadiene
1,3,4,6-tetrachlorocyclohexa-1,4-diene
149665-65-6
CPD-15
CHEBI:513
SCHEMBL2928528
DTXSID80274267
Q27105307
Solubility of 1,3,4,6-tetrachlorocyclohexa-1,4-diene (C6H4Cl4)
The solubility of 1,3,4,6-tetrachlorocyclohexa-1,4-diene, a highly chlorinated cyclic compound, presents some interesting characteristics. Generally, it is known that compounds with multiple chlorine substituents tend to exhibit limited solubility in polar solvents due to their hydrophobic nature.
Key Points about Solubility:
In summary, 1,3,4,6-tetrachlorocyclohexa-1,4-diene (C6H4Cl4) demonstrates a notable degree of solubility in organic solvents while resisting dissolution in polar environments, emphasizing how structural features profoundly influence solubility behaviors.