Synthetic Route of 119515-38-7, The transformation of simple hydrocarbons into more complex and valuable products via catalytic C¨CH bond functionalisation has revolutionised modern synthetic chemistry. 119515-38-7, Name is sec-Butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate, SMILES is O=C(N1C(CCO)CCCC1)OC(C)CC, belongs to piperidines compound. In a article, author is Danko, Martin, introduce new discover of the category.
Synthesis and spectral properties of probes based on pyrene and 2,2,6,6-tetramethylpiperidine-1-H- or 1-oxyl
The spectral properties of novel pyrene-piperidine/pyrene-piperidine-l-oxyl adducts with varying linkers differing in electronic conjugation between these two functionalities were investigated in solvents of different polarity. Tuning their fluorescence efficiency via structure modification is discussed in terms of increased conjugation, solvent polarity effect, main non-radiative de-excitation pathways and static/dynamic excimer or solute-solvent exciplex fluorescence. Compared to parent pyrene molecule, the main additional non-radiative de excitation pathways leading to significant fluorescence quenching were studied using time-resolved fluorescence spectroscopy and quantum-chemical DFT (Density Functional Theory) calculations and were identified as reductive photo-induced electron transfer and intramolecular paramagnetic quenching.
Synthetic Route of 119515-38-7, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 119515-38-7 is helpful to your research.
Reference:
Piperidine – Wikipedia,
,Piperidine | C5H11N – PubChem