Synthetic Route of C5H7N. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: 3-Methyl-1H-pyrrole, is researched, Molecular C5H7N, CAS is 616-43-3, about Theoretical and experimental study of monosubstituted pyrroles. Author is Marey, Therese; Arriau, Jean.
The energies of formation of 2-substituted pyrroles and 3-substituted pyrroles are almost the same; and the wavelengths of the π → π* electronic transition increase in the following order: H < Me < CN < CO2H < CH:NOH < CHO < NO2. Exptl. studies confirm the theoretical relation between wavelength and substituent. The larger bathochromic shifts are observed for the 2-substituted compounds If you want to learn more about this compound(3-Methyl-1H-pyrrole)Synthetic Route of C5H7N, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(616-43-3).
Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate