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![2H-Furo[2,3-c]pyran-2-one - chemical structure image](https://media.scbt.com/product/2h-furo2-3-cpyran-2-one-857054-03-6-structure_29_13_t_291364.jpg "Molecular structure of 2H-Furo[2,3-c]pyran-2-one")
2H-Furo[2,3-c]pyran-2-one (CAS 857054-03-6)
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2H-Furo[2,3-c]pyran-2-one, also referred to as 2H-furo[3,2-c]pyran-2-one, is a significant organic compound widely utilized in scientific research. This heterocyclic compound can be synthesized through diverse methods, including Knoevenagel condensation, Biginelli reaction, aldol condensation, and Fischer indole synthesis. Extensive research has been conducted on this compound to explore its biochemical and physiological effects, as well as its applications in laboratory experiments.The applications of 2H-Furo[2,3-c]pyran-2-one in scientific research are extensive. It has played a role in the synthesis of biologically active compounds such as epothilones, heterocyclic compounds, and polycyclic compounds. Additionally, it has contributed to the synthesis of polymers and materials like polyurethanes, polyamides, and polyesters.
2H-Furo[2,3-c]pyran-2-one (CAS 857054-03-6) References
- Preparation of 2H-furo[2,3-c]pyran-2-one derivatives and evaluation of their germination-promoting activity. | Flematti, GR., et al. 2007. J Agric Food Chem. 55: 2189-94. PMID: 17316021
- Smoke-derived karrikin perception by the α/β-hydrolase KAI2 from Arabidopsis. | Guo, Y., et al. 2013. Proc Natl Acad Sci U S A. 110: 8284-9. PMID: 23613584
- A missense allele of KARRIKIN-INSENSITIVE2 impairs ligand-binding and downstream signaling in Arabidopsis thaliana. | Lee, I., et al. 2018. J Exp Bot. 69: 3609-3623. PMID: 29722815
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2H-Furo[2,3-c]pyran-2-one, 1 mg | sc-394009 | 1 mg | $439.00 |