Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 119515-38-7, Name is sec-Butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate, SMILES is O=C(N1C(CCO)CCCC1)OC(C)CC, in an article , author is Dkhar, Lincoln, once mentioned of 119515-38-7, Product Details of 119515-38-7.
Cp and indenyl ruthenium complexes containing dithione derivatives: Synthesis, antibacterial and antifungal study
A series of cationic complexes [(Cp/Ind)Ru(kappa(2)((SS))-L)(PPh3)]PF6 (1-6) are obtained by the reaction of [CpRu(PPh3)(2)Cl] or [(Ind)Ru(PPh3)(2)Cl] (Cp = eta(5)-C5H5, Ind = eta(5)-C9H7) with respective dithione derivatives 1,2-di(piperidin-1-yl)ethane-1,2-dithione (L1), 1,2-dimorpholinoethane-1,2-dithione (L2) and 1,2-dithiomorpholinoethane-1,2-dithione (L3). All the compounds are characterized using spectroscopic techniques. The molecular structures of complexes 1, 2 and 4 are established by single-crystal X-ray diffraction studies. Antimicrobial studies were tested against three strains of bacterial microorganisms Staphylococcus aureus (gram + ve), Bacillus subtilis (gram + ve), Klebsiella pneumoniae (gram -ve) and one strain of fungal microorganism Candida albicans. (C) 2020 Elsevier B.V. All rights reserved.
But sometimes, even after several years of basic chemistry education, it is not easy to form a clear picture on how they govern reactivity! 119515-38-7, you can contact me at any time and look forward to more communication. Product Details of 119515-38-7.
Reference:
Piperidine – Wikipedia,
,Piperidine | C5H11N – PubChem