24211-36-7 Usage
Uses
Used in Pharmaceutical Industry:
6-DEMETHOXY-ICHTHYNONE is used as a pharmaceutical agent for its estrogenic activity. The compound's ability to mimic the effects of estrogen makes it a potential candidate for the development of drugs targeting hormone-related conditions and diseases.
Used in Agriculture:
6-DEMETHOXY-ICHTHYNONE is used as a natural pesticide and antifungal agent in the agricultural industry. Its insecticidal and antifungal properties make it a valuable tool for controlling pests and diseases in crops, promoting sustainable and environmentally friendly farming practices.
Used in Aquaculture:
In the aquaculture industry, 6-DEMETHOXY-ICHTHYNONE is used as a fish narcotic. Its ability to sedate fish makes it useful for capturing and handling fish in a more humane and efficient manner, reducing stress and injury during transportation and handling processes.
Used in Chemical Research:
6-DEMETHOXY-ICHTHYNONE is used as a research compound in the field of chemical research. Its structural similarity to Berberine (B318150) and other compounds makes it an interesting subject for studying the properties and potential applications of isoflavones and related compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 24211-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,1 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24211-36:
(7*2)+(6*4)+(5*2)+(4*1)+(3*1)+(2*3)+(1*6)=67
67 % 10 = 7
So 24211-36-7 is a valid CAS Registry Number.
24211-36-7Relevant academic research and scientific papers
Total Synthesis of Isoflavones: Jamaicin, Calopogonium Isoflavone-B, Pseudobaptigenin, and Maxima Substance-B. Friedel-Crafts Acylation Reactions with Acid-Sensitive Substrates
Schuda, Paul Francis,Price, William A.
, p. 1972 - 1979 (2007/10/02)
The Friedel-Crafts acylation reaction was studied on several acid-sensitive substrates.Under the proper conditions of varying Lewis acids, solvents, and reaction temperatures, the acylation indeed took place, thus obviating the necessity for functional group protection-deprotection sequences.By use of these procedures, the naturally occuring isoflavones jamaicin (1), calopogonium isoflavone-B (2), maxima substance-B (30), and pseudobaptigenin (31) were synthesized and characterized.
