Molecular structure of Pyrrole, CAS Number: 109-97-7
Pyrrole (CAS 109-97-7)
Application:
Pyrrole is a simple organic molecule that is useful in organic synthesis and many other applications
CAS Number:
109-97-7
Purity:
98%
Molecular Weight:
67.09
Molecular Formula:
C4H5N
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Pyrrole is a heterocyclic compound that functions as a ligand in coordination chemistry, forming complexes with various metal ions. It acts as a π-electron donor, participating in coordination bonds with metal centers to stabilize the resulting complexes. Pyrrole′s mode of action involves the formation of coordination complexes through the lone pair of electrons on the nitrogen atom, allowing it to act as a chelating agent. This enables pyrrole to play a role in the synthesis of metalloporphyrins and related compounds, contributing to the development of novel materials and catalysts.
Pyrrole (CAS 109-97-7) References
- New pyrrole inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity. | La Regina, G., et al. 2007. J Med Chem. 50: 922-31. PMID: 17256833
- Synthesis of certain pyrrole derivatives as antimicrobial agents. | Mohamed, MS., et al. 2009. Acta Pharm. 59: 145-58. PMID: 19564140
- A new pyrrole synthesis via silver(I)-catalyzed cycloaddition of vinylogous diazoester and nitrile. | Billedeau, RJ., et al. 2013. Org Lett. 15: 1421-3. PMID: 23477583
- Living on pyrrolic foundations - Advances in natural and artificial bioactive pyrrole derivatives. | Domagala, A., et al. 2015. Eur J Med Chem. 100: 176-87. PMID: 26087028
- Pyrrole: An emerging scaffold for construction of valuable therapeutic agents. | Gholap, SS. 2016. Eur J Med Chem. 110: 13-31. PMID: 26807541
- New pentasubstituted pyrrole hybrid atorvastatin-quinoline derivatives with antiplasmodial activity. | Carvalho, RC., et al. 2016. Bioorg Med Chem Lett. 26: 1881-4. PMID: 26988303
- Synthesis and Anti-cancer Activity of 3-substituted Benzoyl-4-substituted Phenyl-1H-pyrrole Derivatives. | Zhan, X., et al. 2017. Anticancer Agents Med Chem. 17: 821-831. PMID: 27671311
- 1-Methoxypyrrole-2-carboxamide-A new pyrrole compound isolated from Streptomyces griseocarneus SWW368. | Wattanasuepsin, W., et al. 2017. J Gen Appl Microbiol. 63: 207-211. PMID: 28502957
- Synthesis of Multi-Substituted Pyrrole Derivatives Through [3+2] Cycloaddition with Tosylmethyl Isocyanides (TosMICs) and Electron-Deficient Compounds. | Ma, Z., et al. 2018. Molecules. 23: PMID: 30336556
- Bioactive pyrrole-based compounds with target selectivity. | Li Petri, G., et al. 2020. Eur J Med Chem. 208: 112783. PMID: 32916311
- Identification of a Novel Pyrrole Alkaloid from the Edible Mushroom Basidiomycetes-X (Echigoshirayukidake). | Sakamoto, T., et al. 2020. Molecules. 25: PMID: 33105737
- Therapeutic potential of pyrrole and pyrrolidine analogs: an update. | Jeelan Basha, N., et al. 2022. Mol Divers. 26: 2915-2937. PMID: 35079946
- A Comprehensive Review on Journey of Pyrrole Scaffold Against Multiple Therapeutic Targets. | Mir, RH., et al. 2022. Anticancer Agents Med Chem. 22: 3291-3303. PMID: 35702764
- Four Routes to 3-(3-Methoxy-1,3-dioxopropyl)pyrrole, a Core Motif of Rings C and E in Photosynthetic Tetrapyrroles. | Chau Nguyen, K., et al. 2023. Molecules. 28: PMID: 36770988
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MetAP-2.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Pyrrole, 25 ml | sc-250820 | 25 ml | $29.00 | |||
Pyrrole, 100 ml | sc-250820A | 100 ml | $82.00 |