66056-19-7 Usage
Uses
Used in Pharmaceutical Industry:
Licoisoflavone A is used as a therapeutic agent for its potential effects on various diseases, such as cancer, diabetes, and cardiovascular disorders. Its anti-inflammatory, antioxidant, and antiviral properties contribute to its potential as a natural remedy for these conditions.
Used in Cosmetics Industry:
Licoisoflavone A is used as an active ingredient in skincare products for its anti-inflammatory and antioxidant properties, which can help reduce inflammation and protect the skin from oxidative stress.
Used in Nutraceutical Industry:
Licoisoflavone A is used as a dietary supplement for its potential health benefits, including its neuroprotective and anti-allergic properties, as well as its potential to support overall health and well-being.
Used in Drug Development:
Licoisoflavone A is used as a lead compound in the development of new drugs for the treatment of various medical conditions, leveraging its diverse biological activities and potential therapeutic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 66056-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,5 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66056-19:
(7*6)+(6*6)+(5*0)+(4*5)+(3*6)+(2*1)+(1*9)=127
127 % 10 = 7
So 66056-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C20H18O6/c1-10(2)3-4-13-15(22)6-5-12(19(13)24)14-9-26-17-8-11(21)7-16(23)18(17)20(14)25/h3,5-9,21-24H,4H2,1-2H3
66056-19-7Relevant academic research and scientific papers
Synthesis of Licoisoflavone A and Related Compounds
Tsukayma, Masao,Fujimoto, Kunihiro,Horie, Tokunaru,Masumura, Mitsuo,Nakayama, Mitsuru
, p. 136 - 141 (2007/10/02)
2',4',5,7-Tetrahydroxyisoflavone was partially benzoylated with benzoyl chloride to give 7-benzoyloxy-2',4',5-trihydroxyisoflavone.The condensation of the 7-(benzoyloxy)isoflavone with 2-methyl-3-buten-2-ol, followed by the hydrolysis of the resultant 3'-(3-methyl-2-butenyl)isoflavone gave licoisoflavone A.Its 5'-(3-methyl-2-butenyl) isomer was also synthesized from 5-benzoyloxy-2',4',7-trihydroxyisoflavone in a similar manner.
SYNTHESES OF LICOISOFLAVONE A AND 5'-ALKENYL ISOMER
Tsukayama, Masao,Fujimoto, Kunihiro,Horie, Tokunaru,Yamashita, Yoshiro,Masumura, Mitsuo,Nakayama, Mitsuru
, p. 675 - 678 (2007/10/02)
2',4',5,7-Tetrahydroxyisoflavone was partially benzoylated with benzoyl chloride to give 7-benzoyloxy-2',4',5-trihydroxyisoflavone.The condensation of 7-benzoyloxyisoflavone with 2-methyl-3-buten-2-ol, followed by the hydrolysis of the resultant 3'-(3-met
