In 1989,Journal of Organic Chemistry included an article by Bui The Khai; Arcelli, Antonio. Related Products of 7116-36-1. The article was titled 《A new hydrogen source. 3. Chemoselective reduction with triethylammonium hypophosphite hydrate/Raney nickel and tris(triphenylphosphine)ruthenium dichloride reagents.》. The information in the text is summarized as follows:
Et3NH+ H2PO2-.nH2O (I) acts as a NaH2PO2·H2O modified reagent. Some advantages are noted, including higher product selectivity. Pure aromatic and aliphatic aldehydes are obtained from nitriles by the I/Raney nickel system. The homogeneous catalyst can be used with this reagent. The I/RuCl2(PPh3)3 system selectively reduces aromatic and aliphatic ketones to the corresponding alcs. with excellent yields at room temperature After reading the article, we found that the author used Ethyl 3-(4-chlorophenyl)propanoate(cas: 7116-36-1Related Products 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.Related Products of 7116-36-1
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics