The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate( cas:2199-44-2 ) is researched.Safety of Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate.Arranja, Claudia T.; Ramos Silva, Manuela; Matos Beja, Ana; Ferreira, Ana F. P. V.; Sobral, Abilio J. F. N. published the article 《Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxylate》 about this compound( cas:2199-44-2 ) in Acta Crystallographica, Section E: Structure Reports Online. Keywords: ethyl dimethylpyrrole carboxylate ester crystal structure; mol structure ethyl dimethylpyrrolecarboxylate ester; hydrogen bond dimer ethyl dimethylpyrrolecarboxylate ester. Let’s learn more about this compound (cas:2199-44-2).
In the title compound, C9H13NO2, there are two independent mols. per asym. unit. The mols. are very similar and almost planar, with the ethoxycarbonyl group anti to the pyrrole N atom. The two independent mols. are joined into dimeric units by strong hydrogen bonds between NH groups and carbonyl O atoms. Crystallog. data are given.
There is still a lot of research devoted to this compound(SMILES：O=C(C1=C(C)C=C(C)N1)OCC)Safety of Ethyl 3,5-Dimethyl-2-pyrrolecarboxylate, and with the development of science, more effects of this compound(2199-44-2) can be discovered.
Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com