69684-72-6 Usage
Uses
Used in Pharmaceutical Applications:
(3aR,6aS)-3aβ,5,6,7aβ,7bβ,8a,8bβ,8cα-Octahydro-4β-acetoxy-6β-hydroxy-6,8aβ-dimethyl-3-methylene-4H-bisoxireno[1,8a:2,3]azuleno[4,5-b]furan-2(3H)-one is used as a pharmaceutical candidate for its unique properties and potential applications. Its complex structure and functional groups make it a promising molecule for the development of new drugs and therapies.
Used in Medicinal Chemistry Research:
(3aR,6aS)-3aβ,5,6,7aβ,7bβ,8a,8bβ,8cα-Octahydro-4β-acetoxy-6β-hydroxy-6,8aβ-dimethyl-3-methylene-4H-bisoxireno[1,8a:2,3]azuleno[4,5-b]furan-2(3H)-one is used in medicinal chemistry research to study its structure-activity relationships and explore its potential as a lead compound for the development of new pharmaceutical agents. Its unique core structure and stereochemistry make it an interesting target for further investigation and optimization.
Used in Organic Synthesis:
(3aR,6aS)-3aβ,5,6,7aβ,7bβ,8a,8bβ,8cα-Octahydro-4β-acetoxy-6β-hydroxy-6,8aβ-dimethyl-3-methylene-4H-bisoxireno[1,8a:2,3]azuleno[4,5-b]furan-2(3H)-one is used in organic synthesis to develop new synthetic routes and methods for the preparation of complex organic molecules. Its unique structural features and functional groups provide opportunities for the exploration of novel synthetic strategies and the development of new chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 69684-72-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,8 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69684-72:
(7*6)+(6*9)+(5*6)+(4*8)+(3*4)+(2*7)+(1*2)=186
186 % 10 = 6
So 69684-72-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H20O7/c1-6-9-8(21-7(2)18)5-15(3,20)17-11(10(9)22-14(6)19)16(4)12(23-16)13(17)24-17/h8-13,20H,1,5H2,2-4H3/t8-,9+,10-,11-,12-,13+,15+,16+,17-/m0/s1
69684-72-6Relevant academic research and scientific papers
Jakupovic,Klemeyer,Bohlmann,Graven
, p. 1129 - 1133 (1988)
Artemisia afra afforded in addition to several known compounds 10 new guaianolides and five glaucolides as well as 12-hydroxy-α-cyperone. The structures were elucidated by high field NMR techniques and some chemical transformations.
