2,2-Dimethyl-6-phenylpyrano[3,4-b]pyran-8-one

2,2-Dimethyl-6-phenylpyrano[3,4-b]pyran-8-one
Product Name 2,2-Dimethyl-6-phenylpyrano[3,4-b]pyran-8-one
CAS No.: 1153624-36-2
Catalog No.: CFN96978
Molecular Formula: C16H14O3
Molecular Weight: 254.28 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Oil
Source: The metabolites of Hypericum revolutum ssp.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
2,2-Dimethyl-6-phenylpyrano[3,4-b]pyran-8-one is a natural product from the metabolites of Hypericum revolutum ssp.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
  • Journal of Medicinal Food2023, Vol.26(10).
  • Phytomedicine.2023, 114:154813.
  • Int J Mol Sci.2022, 23(21):13112.
  • J Pharm Biomed Anal.2021, 196:113931.
  • Appl. Sci.2020, 10,1304
  • Food Sci Biotechnol.2023, 32(7):997-1003.
  • Int J Mol Sci.2023, 24(15):12397.
  • J Agric Food Chem.2024, 72(15):8784-8797.
  • Chem Biol Interact.2024, 403:111249.
  • Tokyo Pharmaceutical University2020, 500001431953.
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    METHODS AND RESULTS:
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    CONCLUSIONS:
    Compound 1 exhibited a minimum inhibitory concentration (MIC) of 256 microg/ml, whereas compound 2 was inactive at a concentration of 512 microg/ml.
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