Rabdoketone B
Reference standards.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
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.
Food Funct.2022, 13(14):7638-7649.
BMC Pharmacol Toxicol.2018, 19(1):5
Int J Mol Sci.2023, 24(8):7045.
Prev Nutr Food Sci.2024, 29(4):504-511.
Hum. Ecol. Res.2025, 63(2):165-174
Mol Biol Rep.2024, 51(1):117.
Plos One.2020, 10.1371
Int J Mol Sci.2020, 21(6):2190.
J Chromatogr A.2017, 1518:46-58
University of Stuttgart2021, 11682.
Related and Featured Products
The Journal of Organic Chemistry, 2011, 76(19):8131-8137.
A Sulfone-Based Strategy for the Preparation of 2,4-Disubstituted Furan Derivatives.[Reference:
WebLink]
METHODS AND RESULTS:
2,4-Disubstituted furans are prepared by treating 2,3-dibromo-l-phenylsulfonyl-l-propene (DBP, 2) with 1,3-diketones under basic conditions. The furan-forming step involves a deacetylation, and the selectivity of this process depends upon the steric demand of the R group. The substituent in position 4 is elaborated by reaction of sulfonyl carbanions with alkyl halides, acyl halides, and aldehydes. Oxidative or reductive desulfonylation produces the 24-disubstituted furans in 60-92% yield.
CONCLUSIONS:
This strategy has been used to prepare rabdoketone A (12) and the naturally occurring nematotoxic furoic acid 13.
