Epoxypropyl p-tolyl ether
- Molecular formula
- C10H12O2
- CAS Number
- 2210-74-4
- IUPAC Name
- 2-[(4-methylphenoxy)methyl]oxirane
- Molecular Weight
- 164.20g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0800g/cm3
- Synonyms
- 2186-24-5
Identification
Interesting Facts about 2-[(4-methylphenoxy)methyl]oxirane
2-[(4-methylphenoxy)methyl]oxirane, often referred to as a type of epoxide, is a fascinating compound in organic chemistry due to its unique structure and reactivity. This compound features an oxirane (epoxide) ring that is an intriguing area of study for chemists focused on ring-opening reactions and the development of new synthetic pathways.
Key Characteristics:
- Reactivity: The strained three-membered oxirane ring is highly reactive, making it a valuable building block in organic synthesis.
- Applications in Synthesis: It serves as a precursor for various chemical reactions, including the creation of alcohols, amines, and carboxylic acids.
- Biological Activity: Compounds with similar structures are often investigated for their potential pharmaceutical applications, such as anti-inflammatory and anticancer properties.
In addition, the presence of the 4-methylphenoxy group contributes to its chemical properties, influencing solubility and reactivity, which can be tailored for specific applications. As noted in various studies, "the integration of functional groups allows for greater versatility and innovation in compound design."
This flexibility makes 2-[(4-methylphenoxy)methyl]oxirane an exciting topic for research and exploration in both academic and industrial contexts.
Overall, the compound’s functional characteristics and potential applications underscore the importance of understanding chemical structures and their implications in various fields such as materials science, pharmaceuticals, and agrochemicals.