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- Molecular formula
- C14H14O
- CAS Number
- 119-53-9
- IUPAC Name
- 3-(1-methyl-1-phenyl-ethyl)phenol
- Molecular Weight
- 212.26g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0678g/cm3
- Synonyms
- m-cumylphenol
Identification
Interesting facts
Interesting Facts about 3-(1-methyl-1-phenyl-ethyl)phenol
3-(1-methyl-1-phenyl-ethyl)phenol, often referred to in scientific literature, is a fascinating organic compound with a range of interesting properties and applications. Here are some noteworthy facts:
- Structural Diversity: This compound is an example of a substituted phenol, which means that it has a phenolic ring with an additional alkyl side chain. The presence of the bulky 1-methyl-1-phenyl-ethyl group significantly influences its chemical behavior.
- Biological Activity: Compounds like 3-(1-methyl-1-phenyl-ethyl)phenol are often studied for their potential biological applications. Some derivatives have been found to exhibit antioxidant properties, which could be beneficial in various pharmaceutical contexts.
- Applications in Industry: Due to the functionality provided by the phenolic group, this compound (and its derivatives) may find applications in the production of polymers, resins, and coatings. Phenols are known for their ability to form strong bonds, enhancing durability.
- Research Significance: This compound is of interest in organic synthesis and medicinal chemistry. Researchers utilize it to explore modifications that could enhance functionality or reduce toxicity in drug formulations.
- Environmental Impact: Understanding the environmental behavior of compounds like 3-(1-methyl-1-phenyl-ethyl)phenol is vital as it allows scientists to evaluate their persistence, bioaccumulation potential, and effects on ecosystems.
In conclusion, 3-(1-methyl-1-phenyl-ethyl)phenol is not just a simple chemical entity; it embodies a wealth of possibilities in both scientific research and industrial applications. Its unique structure and properties make it a compound of considerable interest within the field of chemistry.