Model investigations on the mechanism of the osazone reaction. II was written by Dyong, Ingolf;Bertram, H. Peter. And the article was included in Chemische Berichte in 1973.Safety of Ethyl 2-hydroxy-3-phenylpropanoate This article mentions the following:
The aldehydes PhCHRCH(OH)CHO (I, R = OH) (II) and I (R = H) (III) behaved completely differently in reactions with hydrazine derivatives II yielded only the phenylhydrazone and, with difficulty, the derivative PhCOC(:NNPhMe)CH:NNPhMe. III reacted easily to give the derivatives PhCH2C(:NR)CH:NR [R = NHPh, NHC6H3(NO2)2-2,4, NPhMe]. The different reactivities were interpreted on the basis of a Weygand mechanism. In the experiment, the researchers used many compounds, for example, Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0Safety of Ethyl 2-hydroxy-3-phenylpropanoate).
Ethyl 2-hydroxy-3-phenylpropanoate (cas: 15399-05-0) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Safety of Ethyl 2-hydroxy-3-phenylpropanoate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics