2-Phenoxyethyl propanoate

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Identification

Molecular formula
C11H14O3
CAS Number
14248-68-7
IUPAC Name
2-phenoxyethyl propanoate
Molecular Weight
194.24g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0678g/cm3
Synonyms
2-Phenoxyethyl propionate
Interesting facts

Interesting Facts About 2-phenoxyethyl propanoate

2-phenoxyethyl propanoate is an intriguing compound that belongs to the family of ester compounds. Esters are formed through the reaction between an alcohol and an acid, and they play an important role in both synthetic chemistry and the natural world.

Key Characteristics

  • Synthetic Applications: This compound is frequently utilized in organic synthesis, serving as a versatile intermediate in the production of various chemical entities.
  • Fragrance and Flavor: Esters, including 2-phenoxyethyl propanoate, are often characterized by their pleasant aromas and are commonly found in fragrances and flavoring agents, contributing to a range of products you may encounter in daily life.
  • Biochemical Relevance: Understanding esters is fundamental in the field of biochemistry, as many biological molecules involve ester linkages, influencing processes such as lipid formation and energy storage.

Applications

Beyond its use in synthesis, 2-phenoxyethyl propanoate finds its way into various formulations, including:

  • Cosmetics and personal care products
  • Aromatherapy and essential oil blends
  • Pharmaceutical applications as an ingredient in drug formulations

Quote from the Field

As the eminent chemist Robert H. Grubbs once said, "Chemistry is a science of transformation, and every compound carries a story of its creation." 2-phenoxyethyl propanoate exemplifies this transformation, showcasing the beauty and utility of esters in chemical science.

This compound not only highlights the interconnection between chemical structure and functional application but also invites chemists and students alike to explore the vast possibilities that esters present in both industrial and academic contexts.

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