Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Canadian Journal of Chemistry called Pyrrole chemistry. XIII. New syntheses of 3-alkylpyrroles, Author is Groves, J. K.; Anderson, Hugh J.; Nagy, H., which mentions a compound: 616-43-3, SMILESS is CC1=CNC=C1, Molecular C5H7N, Quality Control of 3-Methyl-1H-pyrrole.
3-n-Alkylpyrroles are prepared in good yield by a combined Wolff-Kishner reduction and hydrolysis and decarboxylation of 4-acyl-2-pyrrole-thiolcarboxylates. Me 4-isopropyl-2-pyrrolecarboxylate and 4-tert-butyl-2-pyrrolecarbonitrile are prepared by alkylation of Me 2-pyrrolecarboxylate and 2-pyrrolecarbonitrile, resp. Hydrolysis and decarboxylation of these disubstituted compounds afford the corresponding-3-alkylpyrroles. Mass spectral data for some 1-, 2-, and 3-alkylpyrroles are reported.
In some applications, this compound(616-43-3)Quality Control of 3-Methyl-1H-pyrrole is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.
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