Category: 15399-05-0

Ley, Steven V. et al. published their research in Organic Letters in 2003 | CAS: 15399-05-0

Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Computed Properties of C11H14O3

Recyclable Polyurea-Microencapsulated Pd(0) Nanoparticles: An Efficient Catalyst for Hydrogenolysis of Epoxides was written by Ley, Steven V.;Mitchell, Claire;Pears, David;Ramarao, Chandrashekar;Yu, Jin-Quan;Zhou, Wuzong. And the article was included in Organic Letters in 2003.Computed Properties of C11H14O3 This article mentions the following:

Palladium nanoparticles (∼2 nm in size) microencapsulated in polyurea is an efficient and recyclable catalyst for reductive ring-opening hydrogenolysis of epoxides, using either HCOOH/Et3N or H2 as a hydrogen donor. In the experiment, the researchers used many compounds, for example, Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0Computed Properties of C11H14O3).

Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Computed Properties of C11H14O3

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Mahmout, Yaya et al. published their research in Journal de la Societe Ouest-Africaine de Chimie in 2001 | CAS: 15399-05-0

Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Recommanded Product: Ethyl 2-hydroxy-3-phenylpropanoate

Volatile components of Borassus aethiopum was written by Mahmout, Yaya;Mbaiguinam, Mbailao;Bessiere, Jean-Marie. And the article was included in Journal de la Societe Ouest-Africaine de Chimie in 2001.Recommanded Product: Ethyl 2-hydroxy-3-phenylpropanoate This article mentions the following:

The essential oil and the methylene chloride extract of the pulp of B. aethiopum of Chad were analyzed. The essential yield of the samples was 0.5-0.7%, while methylene chloride extracts gave 1.3% of the residue. The essential oil was characterized by (E)-Et cinnamate and geranylacetone (10.5%) with lesser amounts of 3-phenylpropanol (8.6%) and farnesylacetone (5%). The other main esters were Et 3-hydroxybutanoate (3.4%), Et 3-phenylpropanoate (2.7%), Et benzoate (1.7%), (E)-Me cinnamate (0.8%), Et 3-hydroxyisohexanoate (0.6%) and phenylethyl tiglate (0.6%). The richness of ester compounds may have contributed significantly to the pleasant odor of the ripe fruits of B. aethiopum. The presence of (E)-Et cinnamate in the oil of B. aethiopum was the most major difference noticed on comparison of the essential oil of samples from Sudan. Most of the identified components were not previously known to be present in the volatile extracts of B. aethiopum. These compositional differences may be chemotaxonomically significant. In the experiment, the researchers used many compounds, for example, Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0Recommanded Product: Ethyl 2-hydroxy-3-phenylpropanoate).

Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Recommanded Product: Ethyl 2-hydroxy-3-phenylpropanoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics