Molecular structure of 2(5H)-Furanone, CAS Number: 497-23-4
2(5H)-Furanone (CAS 497-23-4)
Alternate Names:
γ-Crotonolactone; 2-Buten-1,4-olide
CAS Number:
497-23-4
Molecular Weight:
84.07
Molecular Formula:
C4H4O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
2(5H)-Furanone is a heterocyclic organic compound. This colorless liquid possesses solubility in most organic solvents. 2(5H)-Furanone demonstrates numerous scientific research applications, particularly in the synthesis of natural products such as terpenes, steroids, and alkaloids. Additionally, 2(5H)-Furanone serves as a ligand in coordination chemistry and functions as a reagent in organic synthesis. As an electrophile, 2(5H)-Furanone possesses the ability to react with nucleophiles, leading to the formation of covalent bonds. This reaction involves the creation of a carbon-oxygen bond, which gains stability through resonance. It is recognized as a nucleophilic addition reaction.
2(5H)-Furanone (CAS 497-23-4) References
- Alpha-pyrones and a 2(5H)-furanone from Hyptis pectinata. | Boalino, DM., et al. 2003. Phytochemistry. 64: 1303-7. PMID: 14599529
- [2 + 2] Photocycloaddition of 2(5H)-furanone to unsaturated compounds. insights from first principles calculations and transient-absorption measurements. | Cucarull-González, JR., et al. 2010. J Org Chem. 75: 4392-401. PMID: 20518511
- 2(5H)-Furanone: A Prospective strategy for biofouling-control in membrane biofilm bacteria by quorum sensing inhibition. | Ponnusamy, K., et al. 2010. Braz J Microbiol. 41: 227-34. PMID: 24031485
- 2(5H)-Furanone, epigallocatechin gallate, and a citric-based disinfectant disturb quorum-sensing activity and reduce motility and biofilm formation of Campylobacter jejuni. | Castillo, S., et al. 2015. Folia Microbiol (Praha). 60: 89-95. PMID: 25231135
- Unraveling the Molecular Mechanism of Selective Antimicrobial Activity of 2(5H)-Furanone Derivative against Staphylococcus aureus. | Sharafutdinov, IS., et al. 2019. Int J Mol Sci. 20: PMID: 30736278
- A Divergent Paired Electrochemical Process for the Conversion of Furfural Using a Divided-Cell Flow Microreactor. | Cao, Y., et al. 2021. ChemSusChem. 14: 590-594. PMID: 33305485
- Characterization of Key Odorants in Scallion Pancake and Investigation on Their Changes during Storage. | Liu, B., et al. 2021. Molecules. 26: PMID: 34946729
- Anticancer and Apoptotic Activity in Cervical Adenocarcinoma HeLa Using Crude Extract of Ganoderma applanatum. | Kiddane, AT., et al. 2022. Curr Issues Mol Biol. 44: 1012-1026. PMID: 35723290
- A Brominated Furanone Inhibits Pseudomonas aeruginosa Quorum Sensing and Type III Secretion, Attenuating Its Virulence in a Murine Cutaneous Abscess Model. | Muñoz-Cázares, N., et al. 2022. Biomedicines. 10: PMID: 36009394
- Novel Insight into the Volatile Profile and Antioxidant Properties of Crocus sativus L. Flowers. | Cerdá-Bernad, D., et al. 2022. Antioxidants (Basel). 11: PMID: 36139726
- Bringing Antimicrobial Strategies to a New Level: The Quorum Sensing System as a Target to Control Streptococcus suis. | Xue, B., et al. 2022. Life (Basel). 12: PMID: 36556371
- Chemical Composition Profiling and Antifungal Activity of Saffron Petal Extract. | Naim, N., et al. 2022. Molecules. 27: PMID: 36557875
- Investigation of aroma characteristics of seven Chinese commercial sunflower seed oils using a combination of descriptive Analysis, GC-quadrupole-MS, and GC-Orbitrap-MS. | Liu, J., et al. 2023. Food Chem X. 18: 100690. PMID: 37179977
- Variation in mouse chemical signals is genetically controlled and environmentally modulated. | Stopková, R., et al. 2023. Sci Rep. 13: 8573. PMID: 37237091
Activator of:
Olfr906.Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2(5H)-Furanone, 1 g | sc-251889 | 1 g | $54.00 | |||
2(5H)-Furanone, 5 g | sc-251889A | 5 g | $262.00 |