73211-11-7 Usage
Uses
Used in Pharmaceutical Industry:
(3S,4aR,6R,10R,13aR)-3-Acetoxy-1,2,3,4,4a,5,6,9,10,11,12,13a-dodecahydro-6-hydroxy-4,4,13a-trimethyl-9-methylene-10,7-metheno-7H-benzocycloundecene-8,13-dione is used as a potential candidate for the development of pharmaceutical agents due to its potential anticancer, anti-inflammatory, and antimicrobial properties. Further research and testing are required to fully understand its functions and potential applications in this industry.
Used in Research and Development:
(3S,4aR,6R,10R,13aR)-3-Acetoxy-1,2,3,4,4a,5,6,9,10,11,12,13a-dodecahydro-6-hydroxy-4,4,13a-trimethyl-9-methylene-10,7-metheno-7H-benzocycloundecene-8,13-dione is also used in research and development settings to explore its biological activities and potential applications in various fields. The complex structure and multiple functional groups present in the molecule make it an interesting subject for scientific investigation and the development of new therapeutic agents or other applications.
Check Digit Verification of cas no
The CAS Registry Mumber 73211-11-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,1 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73211-11:
(7*7)+(6*3)+(5*2)+(4*1)+(3*1)+(2*1)+(1*1)=87
87 % 10 = 7
So 73211-11-7 is a valid CAS Registry Number.
InChI:InChI=1/C22H30O5/c1-12-14-6-7-18(25)22(5)9-8-19(27-13(2)23)21(3,4)17(22)11-16(24)15(10-14)20(12)26/h10,14,16-17,19,24H,1,6-9,11H2,2-5H3
73211-11-7Relevant academic research and scientific papers
Asymmetric Total Syntheses of 8,9-Seco-ent-kaurane Diterpenoids Enabled by an Electrochemical ODI-[5+2] Cascade
Ding, Hanfeng,Gao, Beiling,Liu, Zhaobo,Tong, Zhenzhong,Wang, Bingnan
supporting information, p. 14892 - 14896 (2021/06/08)
An electrochemical ODI-[5+2] cascade reaction was developed which enables the rapid assembly of diversely functionalized bicyclo[3.2.1]octadienones from sensitive ethynylphenols. By combining a directed retro-aldol/aldol process, a [2,3]-sigmatropic rearr
Terpenoids. XLVIII. New Diterpenoids from Rabdosia shikokiana var. occidentalis
Node, Manabu,Ito, Nozomu,Uchida, Itsuo,Fujita, Eiichi,Fuji, Kaoru
, p. 1029 - 1033 (2007/10/02)
Five new kaurene-type diterpenoids, shikoccin (1), O-methylshikoccin (2), epoxyshikoccin (3), O-methylepoxyshikoccin (4) and shikoccidin (5) were isolated from Rabdosia shikokiana var. occidentalis.All these compounds except for 5 possess a hitherto unknown 8,9-seco-ent-kaurene skeleton.Keywords-Rabdosia shikokiana; diterpenoid; shikoccin; shikoccidin; ent-kaurene; Labiatae
