Synthetic Route of 20737-42-2, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 20737-42-2, Name is 3-Oxo-3,4-dihydropyrazine-2-carboxylic acid, SMILES is O=C(C1=NC=CNC1=O)O, belongs to Pyrazines compound. In a article, author is Golla, Ramesh, introduce new discover of the category.
Synthesis, photophysical, electrochemical properties and crystal structures and Hirschfeld surface analysis of 4 ‘-dimethoxyphenyl-(2,6-di-2-pyrazinyl) pyridines
Four new 4′-dimethoxyphenyl-(2,6-di-2-pyrazinyl) pyridines (1-4) were synthesised by a facile one-pot method using 2-acetylpyrazine and n,n’-dimethoxybanzaldehydes. All compounds (1-4) were characterised by H-1 and C-13{H-1} NMR, and FT-IR spectroscopy. The molecular structure of compounds 1, 2, and 3 was also confirmed by single crystal X-ray diffraction. There exists CH center dot center dot center dot N, CH center dot center dot center dot O and C center dot center dot center dot C aromatic stacking type of intermolecular secondary interactions which resulted into supramolecular structures in compounds 1-3. The Hirshfeld surface analysis was carried out for the confirmation of intermolecular secondary interactions. The dihedral angles between substituted dimethoxyphenyl ring (B) and central pyridine (A) and pyrazine rings (C and D) are in the range of 33-45 degrees. The photophysical properties were studied by UV-Visible and fluorescence spectroscopy and electrochemical properties by cyclic voltammetry. In the UV-Visible spectra, the compounds, 1-4 showed two strong bands at lambda(max), 236-238 and 284-293 nm attributed to the intramolecular charge transfer (pi-pi*) transitions. When these compounds were excited at 350 nm observed emission bands at lambda(em), 463, 511, 462, and 407 nm respectively. The compounds, 1-3 were showed an oxidation peak, (E-OX, 1.18, 1.57 and 1.25 V) but compound 4 showed two oxidation peaks (E-OX, 1.20 and 1.84 V). Astonishingly, only compound, 3 have shown a reduction peak at (E-red, 1.33 V) but there was no reduction peak in 1, 2 and 4. This shows that the compound, 3 undergo reversible redox reaction. (C) 2019 Elsevier B.V. All rights reserved.
Synthetic Route of 20737-42-2, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 20737-42-2.