23370-16-3 Usage
Description
Chrysosplenol C is a trimethoxyflavone that is the 3,7,3'-trimethyl ether derivative of quercetagetin. It is a naturally occurring compound with potential applications in various fields due to its unique chemical structure and properties.
Uses
Used in Pharmaceutical Industry:
Chrysosplenol C is used as a pharmaceutical compound for its potential therapeutic effects. Its chemical structure allows it to interact with various biological targets, making it a candidate for the development of new drugs.
Used in Cosmetic Industry:
Chrysosplenol C is used as an active ingredient in the cosmetic industry for its potential benefits to skin health. Its antioxidant and anti-inflammatory properties may contribute to the development of skincare products that promote healthy and youthful skin.
Used in Research and Development:
Chrysosplenol C is used as a research compound for studying its chemical properties, biological activities, and potential applications in various fields. Its unique structure and properties make it an interesting subject for scientific investigation and the development of new technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 23370-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,7 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23370-16:
(7*2)+(6*3)+(5*3)+(4*7)+(3*0)+(2*1)+(1*6)=83
83 % 10 = 3
So 23370-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H16O8/c1-23-10-6-8(4-5-9(10)19)17-18(25-3)16(22)13-11(26-17)7-12(24-2)14(20)15(13)21/h4-7,19-21H,1-3H3
23370-16-3Relevant articles and documents
O-methylation of flavonoids by cell-free extracts of calamondin orange
Brunet, Gunter,Ibrahim, Ragai K.
, p. 741 - 746 (2007/10/02)
Cell-free extracts of calamondin orange (Citrus mitis) catalysed the O-methylation of almost all hydroxyls of a number of flavonoids, indicating the existence in citrus tissues of ortho, meta, para and 3-O-methyltransferases. The latter, hitherto unreported enzyme, catalysed the formation of 3-O-methyl ethers of galangin and quercetin. The stepwise O-methylation of a number of compounds, especially quercetin and quercetagetin, tends to suggest a coordinated sequence of O-methylations on the surface of a multienzyme complex. The methyl acceptor abilities of the flavonoid substrates used are discussed in relation to their hydroxyl substitution patterns and their negative electron density distribution.
