675-10-5
675-10-5
Chemical Structure
4-Hydroxy-6-methyl-2-pyrone
- CAS No.: 675-10-5
- Formula:C6H6O3
- Molecular Weight:126.11
IUPAC Name: 4-hydroxy-6-methyl-2H-pyran-2-one
InChIKey: NSYSSMYQPLSPOD-UHFFFAOYSA-N
SMILES: O=C1C=C(O)C=C(C)O1
Biological Activity: 4-Hydroxy-6-methyl-2-pyrone is an intermediate. 4-Hydroxy-6-methyl-2-pyrone can be used for the synthesis of Hispidin (HY-100618) and antibacterial agents. 4-Hydroxy-6-methyl-2-pyrone can be used for research on bacterial infections, fungal infections, pancreatic adenocarcinoma, squamous cell carcinoma, and tuberculosis[1][2][3][4][5].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Hydroxy-6-methyl-2-pyrone | 99.77% | 4-Hydroxy-6-methyl-2-pyrone is an intermediate. 4-Hydroxy-6-methyl-2-pyrone can be used for the synthesis of Hispidin (HY-100618) and antibacterial agents. 4-Hydroxy-6-methyl-2-pyrone can be used for research on bacterial infections, fungal infections, pancreatic adenocarcinoma, squamous cell carcinoma, and tuberculosis. | ||||||||||||||||||||
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References
- [1]. Thaisrivongs S, et al. Structure-based design of novel HIV protease inhibitors: carboxamide-containing 4-hydroxycoumarins and 4-hydroxy-2-pyrones as potent nonpeptidic inhibitors. Journal of medicinal chemistry. 1995 Sep 01;38(18):3624-37.
- [2]. Gonindard C, et al. Synthetic hispidin, a PKC inhibitor, is more cytotoxic toward cancer cells than normal cells in vitro. Cell biology and toxicology. 1997 Mar;13(3):141-53.
- [3]. Trushina E, et al. Tricyclic pyrone compounds prevent aggregation and reverse cellular phenotypes caused by expression of mutant huntingtin protein in striatal neurons. BMC neuroscience. 2009 Jul 08;10:73.
- [4]. KK V, et al. Synthesis, Characterization, Computational, and Photophysical Investigation of Novel Pyran‐Azo Bridged Benzothiazoles and Their Biological Studies. ChemistrySelect. 2025 Apr;10(13):e202404988.
- [5]. Mojahidi S, et al. Synthesis and in-vitro cytotoxic evaluation of novel pyridazin-4-one derivatives. Archiv der Pharmazie. 2010 May;343(5):310-3.
