Pritykin, L. M.; Selyutin, O. B.; Nikolaev, A. L. published their research in Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii) on December 31 ,1999. The article was titled 《Quantitative evaluation of the conjugation effect in the hydrolysis of para-substituted aromatic acid esters》.Product Details of 7116-36-1 The article contains the following contents:
The rate constants of alk. and acid hydrolysis of 10 series of para-substituted benzoic, cinnamic, phenylpropynoic, biphenylcarboxylic, phenylacetic, and 3-phenylpropionic acids linearly correlate with the population of the pz-orbital of the phenylene C atom bearing the substituent. This parameter can be regarded as a quant. measure of the conjugation effect. The experimental process involved the reaction of Ethyl 3-(4-chlorophenyl)propanoate(cas: 7116-36-1Product Details of 7116-36-1)
Ethyl 3-(4-chlorophenyl)propanoate(cas: 7116-36-1) belongs to organochlorine compounds. The wide structural variety and divergent chemical properties of organochlorides lead to a broad range of names, applications, and properties. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Product Details of 7116-36-1
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Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics