Caraphenol A
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.
Biomed Pharmacother.2021, 139:111585.
Evid Based Complement Alternat Med.2020, 2020:8582318.
The Japan Society for Analy. Chem.2017, 66(8):613-617
J Appl Biol Chem.2024, 67:47,337-343.
Front Pharmacol.2017, 8:673
Molecules2021, 26(1),230
Sci Rep. 2018, 10590
BMC Microbiol.2019, 19(1):78
Biochem Biophys Res Commun.2021, 534:802-807.
Research Square2023, 2883170.
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Angew Chem Int Ed Engl. 2014 Mar 24;53(13):3409-13.
9-Membered carbocycle formation: development of distinct Friedel-Crafts cyclizations and application to a scalable total synthesis of (±)-caraphenol A.[Pubmed:
24677499]
METHODS AND RESULTS:
Explorations into a series of different approaches for 9-membered carbocycle formation have afforded the first reported example of a 9-exo-dig ring closure via a Au(III)-promoted reaction between an alkyne and an aryl ring as well as several additional, unique Friedel-Crafts-type cyclizations. Analyses of the factors leading to the success of these transformations are provided, with the application of one of the developed 9-membered ring closures affording an efficient and scalable synthesis of the bioactive resveratrol trimer Caraphenol A.
CONCLUSIONS:
That synthesis proceeded with an average yield of 89% per step (7.8% overall yield) and has provided access to more than 600 mg of the target molecule.
