941227-27-6 Usage
General Description
"1,3,5-Cadinatriene-3,8-diol" is a natural organic compound that belongs to the class of cadinene sesquiterpenes. It is commonly found in essential oils of various plants such as Eupatorium capillifolium and Laurus nobilis. The chemical structure of 1,3,5-Cadinatriene-3,8-diol consists of a cadinene core with three hydroxyl groups attached at positions 3 and 8. 1,3,5-Cadinatriene-3,8-diol possesses a unique and complex arrangement of carbon and hydrogen atoms that contributes to its distinctive aroma and potential biological activities. 1,3,5-Cadinatriene-3,8-diol has been studied for its antimicrobial, antioxidant, and anti-inflammatory properties, making it a subject of interest for pharmaceutical and cosmetic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 941227-27-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,1,2,2 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 941227-27:
(8*9)+(7*4)+(6*1)+(5*2)+(4*2)+(3*7)+(2*2)+(1*7)=156
156 % 10 = 6
So 941227-27-6 is a valid CAS Registry Number.
941227-27-6Relevant articles and documents
Studies of Australian Soft Corals. XXXVI The Isolation and Structure Determination of 11 Calamenene-Based Sesquiterpenes from Lemnalia cervicornis (Coelenterata, Octocrrallia, Alcyonacea)
Bowden, Bruce F.,Coll, John C.,Engelhardt, Lutz M.,Tapiolas, Dianne M.,White, Allan M.
, p. 103 - 121 (2007/10/02)
The soft coral Lemnalia cervicornis May 1898 has afforded 13 novel sesquiterpenoid metabolites.The majority were derivatives of calamenen-7-ol and the structures were deduced by 1H and 13C n.m.r. spectroscopy.Absolute stereochemistry of compounds (3)-(13) was determined by chemical correlation with 7-hydroxycalamenen-3-one (3) for which an X-ray structure determination of its 7-p-bromobenzoyl derivative is reported.Two minor metabolites (15) and (16) were not aromatic, but were structurally related to the algal metabolite zonarene (21) for which absolute stereochemistry was available.
