Interesting facts
Interesting Facts about 2,2,2-Trichloro-1-(p-tolyl)ethanol
2,2,2-Trichloro-1-(p-tolyl)ethanol is a fascinating compound that finds its significance primarily in the field of science and medicinal chemistry. Here are some notable aspects of this compound:
- Chemical Structure: This compound features a unique structure characterized by the presence of three chlorine atoms attached to the carbon atom adjacent to the hydroxyl group. The p-tolyl group, a methyl-substituted phenyl ring, contributes to its chemical properties and reactivity.
- Pharmacological Relevance: Due to its structural characteristics, 2,2,2-trichloro-1-(p-tolyl)ethanol is studied for its potential applications in medicinal chemistry. Compounds that feature halogen substituents like chlorine are known for their diverse therapeutic effects, including antibacterial and antifungal properties.
- Uses in Organic Synthesis: This compound serves as an important intermediate in organic synthesis, demonstrating its utility in the formation of more complex molecules. Chemists often utilize such intermediates to create various pharmaceuticals and agrochemicals.
- Safety Considerations: As with many halogenated compounds, it's essential to handle 2,2,2-trichloro-1-(p-tolyl)ethanol with care. Proper safety protocols should be observed in laboratory settings due to potential toxicity and environmental impact.
- Understanding Mechanisms: Investigating the behavior of this compound under different conditions can provide insights into reaction mechanisms. Such studies are crucial for advancing knowledge in chemical reactivity and the development of new synthetic methods.
In the world of chemistry, compounds like 2,2,2-trichloro-1-(p-tolyl)ethanol play a vital role in bridging theoretical knowledge and practical applications. As scientists continue to explore its properties and uses, ongoing research promises to unveil even more exciting possibilities.
Synonyms
17936-73-1
2,2,2-trichloro-1-p-tolylethanol
2,2,2-trichloro-1-(4-methylphenyl)ethanol
1-(4-Methylphenyl)-2,2,2-trichloroethanol
BRN 1870865
p-Methyl-alpha-(trichloromethyl)benzyl alcohol
BENZYL ALCOHOL, p-METHYL-alpha-(TRICHLOROMETHYL)-
4-06-00-03243 (Beilstein Handbook Reference)
SCHEMBL11302427
DTXSID60939206
DA-20254
2,2,2-Trichloro-1-(4-methylphenyl)ethan-1-ol
Solubility of 2,2,2-trichloro-1-(p-tolyl)ethanol
The solubility of 2,2,2-trichloro-1-(p-tolyl)ethanol (C10H10Cl3O) is influenced by several factors due to its unique molecular structure. This compound has both hydrophobic and hydrophilic characteristics, leading to varied solubility in different solvents. Here are some key points to consider regarding its solubility:
In summary, the solubility of 2,2,2-trichloro-1-(p-tolyl)ethanol is a complex interplay between its polar functional groups and the non-polar characteristics of the halogen substitutions. Understanding these interactions can guide its applications and usage in various chemical processes.