36804-17-8 Usage
Uses
Used in Pharmaceutical Industry:
Silybin (mixture of silybin A and silybin B) is used as a hepatoprotective agent for its ability to protect the liver from damage caused by toxins, alcohol, and other substances. It is commonly used in traditional medicine for liver disorders.
Used in Dietary Supplements:
Silybin (mixture of silybin A and silybin B) is used as a dietary supplement for its antioxidant, anti-inflammatory, and hepatoprotective properties, as well as for its potential anti-cancer effects and ability to improve skin health.
Used in Cosmetics Industry:
Silybin (mixture of silybin A and silybin B) is used as an ingredient in cosmetic products for its potential skin health benefits, such as improving skin elasticity and reducing the appearance of wrinkles.
Used in Research and Development:
Silybin (mixture of silybin A and silybin B) is used in research and development for its potential anti-cancer effects, with ongoing studies investigating its ability to modulate various oncological signaling pathways and exert inhibitory effects on tumor growth and progression.
Check Digit Verification of cas no
The CAS Registry Mumber 36804-17-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,0 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36804-17:
(7*3)+(6*6)+(5*8)+(4*0)+(3*4)+(2*1)+(1*7)=118
118 % 10 = 8
So 36804-17-8 is a valid CAS Registry Number.
InChI:InChI=1/C25H22O10/c1-32-17-6-11(2-4-14(17)28)24-20(10-26)33-16-5-3-12(7-18(16)34-24)25-23(31)22(30)21-15(29)8-13(27)9-19(21)35-25/h2-9,20,23-29,31H,10H2,1H3/t20?,23-,24?,25+/m0/s1
36804-17-8Relevant academic research and scientific papers
Benzodioxans by Oxidative Phenol Coupling. Synthesis of Silybin
Merlini, Lucio,Zanarotti, Antonio,Pelter, Andrew,Rochefort, Malcolm P.,Haensel, Rudolf
, p. 775 - 778 (2007/10/02)
Oxidative coupling of substituted catechols with isoeugenol or coniferyl alcohol in the presence of silver oxide affords 2,3-trans-1,4-benzodioxans in good yield.The reaction is highly regioselective when the catechol bears an alkyl substituent, much less
