70051-38-6 Usage
General Description
4,10-Aromadendranediol is a natural chemical compound found in plants such as Eucalyptus and Salvia species, and it belongs to the class of diterpenoids. It is known for its anti-inflammatory and analgesic properties, making it a potential candidate for the development of new pharmaceutical drugs. Research has shown that 4,10-Aromadendranediol has the ability to inhibit the production of inflammatory mediators in the body, which could make it useful for treating conditions such as arthritis and other inflammatory diseases. Additionally, it has been found to possess antioxidant properties, which could contribute to its potential therapeutic benefits. Overall, 4,10-Aromadendranediol is a promising natural compound with potential applications in pharmaceutical and medical research.
Check Digit Verification of cas no
The CAS Registry Mumber 70051-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,0,5 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 70051-38:
(7*7)+(6*0)+(5*0)+(4*5)+(3*1)+(2*3)+(1*8)=86
86 % 10 = 6
So 70051-38-6 is a valid CAS Registry Number.
70051-38-6Relevant articles and documents
The synthesis of mono- and dihydroxy aromadendrane sesquiterpenes, starting from natural (+)-aromadendrene-III
Gijsen, Harrie J. M.,Wijnberg, Joannes B. P. A.,Stork, Gerrit A.,De Groot, Aede,De Waard, Maarten A.,Van Nistelrooy, Johannes G. M.
, p. 2465 - 2476 (2007/10/02)
The monoalcohols (-)-globulol (2), (-)-epiglobulol (3), (-)-ledol (4), and (+)-viridiflorol (5) were synthesized from (+)-aromadendrene (1). The cis-fused alloaromandedrone (14), the key intermediate used in the synthesis of 4 and 5, was obtained from the trans-fused apoaromadendrone (13) via a selective protonation of the thermodynamic enol trimethylsilylether 15. After hydroxylation of the tertiary C11 of 13 with RuO4, (+)-spathulenol (6), (-)-allospathulenol (7), and the aromadendrane diols 8-11 could be prepared. Compounds 2-11 were tested for antifungal properties, but their activity was only moderate.
