111200-01-2 Usage
General Description
7α-ethoxyrosmanol is a chemical compound that belongs to the class of diterpenoids, which are organic compounds found in various plants. It is a derivative of rosmanol, a natural phenolic compound which has been identified in rosemary and other herbs, and has been shown to possess antioxidant and anti-inflammatory properties. 7α-ethoxyrosmanol has been studied for its potential health benefits, including its ability to protect cells from oxidative damage and reduce inflammation in the body. Additionally, it has shown potential as a natural preservative in food and cosmetic products due to its antioxidant properties. Studies on this compound continue to explore its potential therapeutic applications and safety for human consumption.
Check Digit Verification of cas no
The CAS Registry Mumber 111200-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,2,0 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 111200-01:
(8*1)+(7*1)+(6*1)+(5*2)+(4*0)+(3*0)+(2*0)+(1*1)=32
32 % 10 = 2
So 111200-01-2 is a valid CAS Registry Number.
111200-01-2Relevant articles and documents
Semisynthesis of rosmanol and its derivatives. Easy access to abietatriene diterpenes isolated from the genus Salvia with biological activities
Marrero, Joaquin G.,Andres, Lucia S.,Luis, Javier G.
, p. 986 - 989 (2007/10/03)
The known diterpenes rosmanoi (3), rosmaquinone (4), 7-methoxyrosmanol (5), 7-ethoxyrosmanol (6), galdosol (7), and epirosmanol (8) have been obtained by partial synthesis from carnosol (2), an abundant natural product present in Salvia species. The physical and spectroscopic data of these semisynthetic diterpenes were identical to those of authentic natural samples and with data reported in the literature. These abietane diterpenes have very interesting biological activities and are present in the genus Salvia in low quantities; thus, the semisynthetic approach described here represents an efficient alternative method to obtain these compounds. Additionally, the known diterpene 16-hydroxyrosmanol (10) and a new aromatic diterpene 11 were obtained from 16-hydroxycarnosol (9) by reaction with Ph3P/NBS in CH2Cl2. The structure of the new compound 11 was established from its spectroscopic data as 12,16-epoxycarnosol.
