6027-43-6 Usage
General Description
Rooibos Extract Aspalathus Linearis, often referred to as "Red Bush" extract, is derived from the Aspalathus Linearis plant, a shrub native to South Africa. This chemical is widely used due to its rich antioxidant content, boasting two flavonoids called Aspalathin and Nothofagin that are not found in any other plant. Notably, it has anti-inflammatory, antimutagenic and antiviral qualities. It is also caffeine-free, low in tannins and high in minerals like calcium, potassium and zinc. Additionally, it contains alpha hydroxy acid, known for promoting healthy skin. Therefore, it's commonly used in skincare products, health supplements and tea.
Check Digit Verification of cas no
The CAS Registry Mumber 6027-43-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6027-43:
(6*6)+(5*0)+(4*2)+(3*7)+(2*4)+(1*3)=76
76 % 10 = 6
So 6027-43-6 is a valid CAS Registry Number.
6027-43-6Relevant articles and documents
Method for the Synthesis of Aspalathin and Analogues Thereof
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Paragraph 0076; 0077; 0078; 0079; 0080; 0081; 0082, (2013/03/26)
A method of synthesising Aspalathin and its analogues or derivatives is disclosed. The method comprises synthesising a compound of formula 1 or its analogues or derivatives: wherein each of R1, R2, R3, R4, Rsub
Concise total syntheses of aspalathin and nothofagin
Yepremyan, Akop,Salehani, Baback,Minehan, Thomas G.
supporting information; experimental part, p. 1580 - 1583 (2010/06/17)
Chemical Fig. Reprentation Syntheses of the C-glycosyl flavone natural products aspalathin and nothofagin have been accomplished in eight steps from tribenzyl glucal, tribenzylphloroglucinol, and either 4-(benzyloxy) phenylacetylene or 3,4-bis(benzyloxy)phenylacetylene. The key step of the syntheses involves a highly stereoselective Lewis acid promoted coupling of 1,2-di-o-acyl-3,4,6-tribenzylglucose with tribenzylphloroglucinol, which gives rise to the corresponding β-C-aryl glycoside in 30-65% yields.
