Huang, Lei et al. published their research in Shandong Huagong in 2016 | CAS: 27249-90-7

Benzyl benzodithioate (cas: 27249-90-7) 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. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Application In Synthesis of Benzyl benzodithioate

UV synthesis PPMM – g – HEMA membrane and characterization was written by Huang, Lei;Yang, Li;Zheng, Lei;Shen, Weicheng. And the article was included in Shandong Huagong in 2016.Application In Synthesis of Benzyl benzodithioate This article mentions the following:

In this paper, using ferric chloride (FeCl3) and benzophenone (BP) as co – photoinitiators, benzyl benzodithioate as chain transfer agent, the UV – induced graft polymerization of hydrophilic 2 – hydroxyethyl methacrylate (HEMA) onto hydrophobic polypropylene microporous membrane ( PPMM) was studied. Influencing factors of synthetic membranes were explored. Furthermore the poly (HEMA) – modified membrane surfaces were characterized by attenuated total reflectance Fourier transform IR spectroscopy . In the experiment, the researchers used many compounds, for example, Benzyl benzodithioate (cas: 27249-90-7Application In Synthesis of Benzyl benzodithioate).

Benzyl benzodithioate (cas: 27249-90-7) 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. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Application In Synthesis of Benzyl benzodithioate

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