Extracurricular laboratory: Synthetic route of 616-43-3

There are many compounds similar to this compound(616-43-3)Safety of 3-Methyl-1H-pyrrole. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

Safety of 3-Methyl-1H-pyrrole. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: 3-Methyl-1H-pyrrole, is researched, Molecular C5H7N, CAS is 616-43-3, about Alkylpyrroles in a kerogen pyrolysate: evidence for abundant tetrapyrrole pigments. Author is Sinninghe Damste, Jaap S.; Eglinton, Timothy I.; de Leeuw, Jan W..

C1-C6 alkylated pyrroles were identified as major constituents of the flash pyrolyzate of a kerogen from the Miocene Monterey Formation (California, USA) using gas chromatog. with an N-selective detector and gas chromatog.-mass spectrometry. The major alkylpyrroles identified are 2,3,4-trimethylpyrrole, 3-ethyl-4-methylpyrrole, 2,3-dimethyl-4-ethylpyrrole, 2,4-dimethyl-3-ethylpyrrole, and 3-ethyl-2,4,5-trimethylpyrrole. The alkyl substitution patterns of the alkylpyrroles strongly suggest an origin from tetrapyrrole pigments. Evidence for this hypothesis was provided by flash pyrolysis of the tetrapyrrole pigments chlorophyll-a, protoporphyrin-IX di-Me ester, and bilirubin, which yielded alkylpyrroles with a similar isomer distribution. Quant. pyrolysis using a polymer internal standard of both the kerogen and the tetrapyrrole pigments revealed that ca. 5% of the kerogen consists of macromolecularly bound tetrapyrrole pigments or that this fraction contains ca. 5% insoluble tetrapyrrole salts. These results show that in specific cases tetrapyrrole pigments can contribute significantly to the sedimentary organic matter.

There are many compounds similar to this compound(616-43-3)Safety of 3-Methyl-1H-pyrrole. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

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