Demethoxycapillarisin

Demethoxycapillarisin
Product Name Demethoxycapillarisin
CAS No.: 61854-36-2
Catalog No.: CFN97716
Molecular Formula: C15H10O6
Molecular Weight: 286.24 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Powder
Source: The roots of Saposhnikovia divaricata
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Reference standards.
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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.
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  • Int J Mol Sci.2021, 22(16):8604.
  • Molecules.2023, 28(4):1526.
  • Biochem Biophys Res Commun.2018, 505(1):194-200
  • Braz J Med Biol Res. 2016, 49(7)
  • The Japan Society for Analytical Chemistry2018, 67(4):201-206
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    Journal of the Chemical Society Chemical Communications, 1981, 12(10).
    Synthesis of demethoxycapillarisin, a naturally occurring 2-phenoxychromone, and related compounds.[Reference: WebLink]

    METHODS AND RESULTS:
    Demethoxycapillarisin (1), a naturally occurring 2-phenoxychromone, and the related compounds (2)–(4) have been synthesized via a route involving, as a key step, an intramolecular Wittig reaction between a phosphorus ylide and a carbonate.
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