41059-80-7 Usage
Uses
Used in Pharmaceutical Industry:
(1aR,4E,7R,7aR,10aS,10bR)-7-Acetoxy-2,3,6,7,7a,8,10a,10b-octahydro-1a,5-dimethyl-8-methyleneoxireno[9,10]cyclodeca[1,2-b]furan-9(1aH)-one is used as a potential pharmaceutical agent for its possible biological activity. (1aR,4E,7R,7aR,10aS,10bR)-7-Acetoxy-2,3,6,7,7a,8,10a,10b-octahydro-1a,5-dimethyl-8-methyleneoxireno[9,10]cyclodeca[1,2-b]furan-9(1aH)-one's unique structure and functional groups may contribute to its efficacy in treating various medical conditions, warranting further research and development in drug discovery.
Used in Synthetic Organic Chemistry:
In the field of synthetic organic chemistry, (1aR,4E,7R,7aR,10aS,10bR)-7-Acetoxy-2,3,6,7,7a,8,10a,10b-octahydro-1a,5-dimethyl-8-methyleneoxireno[9,10]cyclodeca[1,2-b]furan-9(1aH)-one serves as a valuable compound for the synthesis of novel organic molecules. Its complex structure and functional groups provide opportunities for chemical modifications and the development of new synthetic pathways, expanding the scope of organic chemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 41059-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,0,5 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 41059-80:
(7*4)+(6*1)+(5*0)+(4*5)+(3*9)+(2*8)+(1*0)=97
97 % 10 = 7
So 41059-80-7 is a valid CAS Registry Number.
InChI:InChI=1/C17H22O5/c1-9-6-5-7-17(4)15(22-17)14-13(10(2)16(19)21-14)12(8-9)20-11(3)18/h6,12-15H,2,5,7-8H2,1,3-4H3/b9-6+/t12-,13-,14+,15?,17-/m1/s1
41059-80-7Relevant articles and documents
Sesquiterpene lactones and thymol esters from Vicoa pentanema
Mossa, Jaber S.,El-Feraly, Farouk S.,Muhammad, Ilias,Zaw, Kyaw,Mbwambo, Zakaria H.,Pezzuto, John M.,Fong, Harry H. S.
, p. 550 - 555 (1997)
The aerial parts of Vicoa pentanema yielded four new sesquiterpene lactones, namely, 10a-hydroxy- 14H-inuviscolide (1), 4α,5α-epoxy- 10α,11β,13H, 14H-1 -epi-inuviscolide 3-β-D-glucoside (2), 2α-O-acetyl- 3β-hydroxyalantolactone (3), and 2α,3α-dihydroxyalloalantolactone (4). The structure and stereochemical assignments of all sesquiterpenes were based on their 1H and 13C-NMR spectral data, including those derived from 2D-NMR COSY, HETCOR, FLOCK, and NOESY experiments, as well as extensive NOE- difference studies. In addition, the same plant material yielded the known sesquiterpene lactones 8β-hydroxyparthenolide (5), 8-epi-confertin (6), 4α,5α-epoxy-10α,14H-1-epi-inuviscolide (7), inuviscolide (8), lipiferolide (9), and carabrone (10), the known thymol ester 7,8-epoxy-9- (isobutyryloxy)thymolisobutyrate (11), and its hydrolysis product 7-hydroxy- 8,9-bis(isobutyryloxy)thymol (12).
