Interesting facts
              Interesting Facts about Ethyl 3-Phenylpropanoate
Ethyl 3-phenylpropanoate is a fascinating compound that belongs to the family of esters, which are widely recognized for their diverse applications in both the food industry and perfumery. Here are some intriguing aspects of this compound:
- Flavor and Aroma: This ester is known for its fruity and sweet odor, reminiscent of apples and other ripe fruits. As a result, it is often utilized in the creation of artificial flavorings and fragrances.
 - Synthesis: The compound is typically synthesized through the esterification reaction between ethanol and 3-phenylpropanoic acid. This process involves the elimination of water, resulting in the formation of the ester.
 - Natural Occurrence: Ethyl 3-phenylpropanoate can be found in certain essential oils and food items, contributing to their aroma profile. It adds a layer of complexity to flavors in foods such as candies and baked goods.
 - Biological Significance: Some studies have suggested that esters like ethyl 3-phenylpropanoate may play a role in plant signaling, aiding in processes such as pollination by attracting pollinators with their pleasant scents.
 - Research Applications: Given its distinct characteristics, this compound is often studied in organic chemistry for its reactivity and as a precursor for synthesizing other complex molecules.
 
In summary, ethyl 3-phenylpropanoate is not just another ester; it represents a bridge between chemistry and sensory experiences in nature, highlighting how chemical compounds can influence our perception of flavors and scents.
Synonyms
          Ethyl 3-phenylpropionate
          Ethyl 3-phenylpropanoate
          2021-28-5
          Ethyl hydrocinnamate
          Benzenepropanoic acid, ethyl ester
          3-Phenylpropionic Acid Ethyl Ester
          Hydrocinnamic acid, ethyl ester
          ETHYL BENZENEPROPANOATE
          Ethylhydrocinnamoate
          Ethylphenyl propanoate
          FEMA No. 2455
          UNII-58E9Z9V64D
          DTXSID9047095
          58E9Z9V64D
          EINECS 217-966-6
          ethyl beta-phenylpropionate
          NSC 126040
          NSC-126040
          AI3-11591
          DTXCID7027095
          Hydrocinnamic acid, ethyl ester (8CI)
          ETHYL 3-PHENYLPROPIONATE [FHFI]
          EPP cpd
          ethyl phenylpropanoate
          ETHYL BETA-PHENYLPROPANOATE
          217-966-6
          ethyl phenylpropionate
          inchi=1/c11h14o2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-7h,2,8-9h2,1h
          jagzuigghgtfho-uhfffaoysa-n
          Ethyl dihydrocinnamate
          ethyl benzylacetate
          MFCD00009206
          Ethyl3-phenylpropionate
          ethylhydrocinnamate
          3-phenyl-propionic acid ethyl ester
          HYDROCINNAMIC ACID ETHYL ESTER
          ethyl 3phenylpropionate
          Ethyl 3-phenylproprionate
          Ethyl hydrocinnamate, 99%
          SCHEMBL304816
          CHEMBL2252095
          FEMA 2455
          CHEBI:173833
          3-phenylpropanoic acid ethyl ester
          3-phenyl-propanoic acid ethyl ester
          Tox21_302337
          BBL035649
          NSC126040
          STL442490
          AKOS005256946
          CS-W002049
          FE39043
          Ethyl 3-phenylpropionate, >=98%, FG
          NCGC00256223-01
          AC-23568
          CS-11279
          SY013603
          CAS-2021-28-5
          DB-014798
          NS00021817
          P1304
          EN300-7403201
          ETHYL HYDROCINNAMATE;ETHYL B-PHENYLPROPIONATE
          Q27261590
          3-Phenylpropionic acid ethyl ester;Ethyl hydrocinnamate
              
Solubility of Ethyl 3-phenylpropanoate
Ethyl 3-phenylpropanoate, with the chemical formula C11H14O2, exhibits interesting solubility characteristics that are essential to its applications in various fields, particularly in organic synthesis and flavoring. When considering the solubility of this compound, several key factors come into play:
- Ethyl alcohol
 
            - Ethanol
 
            - Acetone
 
        
However, it is insoluble in water due to its hydrophobic benzene ring, which significantly reduces its solubility in polar solvents.In conclusion, while ethyl 3-phenylpropanoate is soluble in many organic solvents, it shows a clear preference for non-polar or weakly polar environments, making it unsuitable for aqueous solutions. This property is quite relevant in industrial applications where the choice of solvent is crucial for efficiency and effectiveness.