3-Acetyl-1-methylpyrrole (CAS 932-62-7)
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3-Acetyl-1-methylpyrrole, denoted as 3-AMP, is an organic compound characterized by its distinct structure and properties. This aliphatic heterocyclic compound features a pyrrole ring system with an attached acetyl group. Within the realm of scientific research, 3-Acetyl-1-methylpyrrole finds extensive application in areas such as synthesis methods, mechanism of action, biochemical and physiological effects, as well as advantages and limitations in laboratory experiments. Notably, 3-Acetyl-1-methylpyrrole has been widely utilized as a model compound in investigations concerning the mechanism of action of acetylcholinesterase, an enzyme responsible for acetylcholine hydrolysis. Additionally, it has been instrumental in studying the structure and properties of polypyrrole derivatives. Furthermore, 3-Acetyl-1-methylpyrrole has served as a model compound to explore the mechanism of action of monoamine oxidase, an enzyme involved in monoamine oxidation.
3-Acetyl-1-methylpyrrole (CAS 932-62-7) References
- Alternative GC-MS approaches in the analysis of substituted pyrazines and other volatile aromatic compounds formed during Maillard reaction in potato chips. | Lojzova, L., et al. 2009. Anal Chim Acta. 641: 101-9. PMID: 19393373
- Calorimetric and computational study of 2- and 3-acetyl-1-methylpyrrole isomers. | Ribeiro da Silva, MA. and Santos, AF. 2010. J Phys Chem B. 114: 2846-51. PMID: 20141148
- Convergent integration of two self-labor domino sequences: a novel method for the synthesis of oxazole derivatives from methyl ketones and benzoins. | Xue, WJ., et al. 2012. Chem Commun (Camb). 48: 3485-7. PMID: 22286368
- Antioxidant activities of extracts from teas prepared from medicinal plants, Morus alba L., Camellia sinensis L., and Cudrania tricuspidata , and their volatile components. | Nam, S., et al. 2012. J Agric Food Chem. 60: 9097-105. PMID: 22871255
- Molecular energetics of alkyl pyrrolecarboxylates: calorimetric and computational study. | Santos, AF. and Ribeiro da Silva, MA. 2013. J Phys Chem A. 117: 5195-204. PMID: 23682652
- Microwave-assisted preparation of azachalcones and their N-alkyl derivatives with antimicrobial activities. | Usta, A., et al. 2014. Nat Prod Res. 28: 483-7. PMID: 24571646
- Synthesis and Screening of New [1,3,4]Oxadiazole, [1,2,4]Triazole, and [1,2,4]Triazolo[4,3-b][1,2,4]triazole Derivatives as Potential Antitumor Agents on the Colon Carcinoma Cell Line (HCT-116). | Abdelrehim, EM. 2021. ACS Omega. 6: 1687-1696. PMID: 33490827
- Photo-on-Demand Synthesis of Vilsmeier Reagents with Chloroform and Their Applications to One-Pot Organic Syntheses. | Liang, F., et al. 2021. J Org Chem. 86: 6504-6517. PMID: 33844541
- Functional Characterization of the GATA-Type Transcription Factor PaNsdD in the Filamentous Fungus Podospora anserina and Its Interplay with the Sterigmatocystin Pathway. | Shen, L., et al. 2022. Appl Environ Microbiol. 88: e0237821. PMID: 35080910
- Synthesis, screening as potential antitumor of new poly heterocyclic compounds based on pyrimidine-2-thiones. | Abdelrehim, EM. and El-Sayed, DS. 2022. BMC Chem. 16: 16. PMID: 35313953
- Structure-activity relationships of (4-acylpyrrol-2-yl)alkanoic acids as inhibitors of the cytosolic phospholipase A2: variation of the substituents in positions 1, 3, and 5. | Lehr, M. 1997. J Med Chem. 40: 3381-92. PMID: 9341913
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Acetyl-1-methylpyrrole, 5 g | sc-231430 | 5 g | $61.00 |