58298-76-3 Usage
Description
(3aR,6Z,9R,10aS,11aS)-2,3,3a,10,10a,11a-Hexahydro-3,3,6,9,11a-pentamethyl-1H-dicyclopenta[a,d]cyclononene-1,5,11(4H,9H)-trione is a complex organic compound characterized by its unique molecular structure. It features a cyclopentanone ring and a cyclopentene ring, with three carbonyl groups making it a trione derivative. (3aR,6Z,9R,10aS,11aS)-2,3,3a,10,10a,11a-Hexahydro-3,3,6,9,11a-pentamethyl-1H-dicyclopenta[a,d]cyclononene-1,5,11(4H,9H)-trione also has six methyl groups attached to the rings, giving it a distinctive pentamethyl structure. Its intricate structure and functional groups suggest potential applications in various fields, such as pharmaceuticals, agricultural chemicals, or material science.
Uses
Used in Pharmaceutical Industry:
(3aR,6Z,9R,10aS,11aS)-2,3,3a,10,10a,11a-Hexahydro-3,3,6,9,11a-pentamethyl-1H-dicyclopenta[a,d]cyclononene-1,5,11(4H,9H)-trione is used as a pharmaceutical compound for its potential therapeutic properties. Its complex structure and functional groups may contribute to the development of new drugs with specific targeting and efficacy.
Used in Agricultural Chemicals:
In the agricultural sector, (3aR,6Z,9R,10aS,11aS)-2,3,3a,10,10a,11a-Hexahydro-3,3,6,9,11a-pentamethyl-1H-dicyclopenta[a,d]cyclononene-1,5,11(4H,9H)-trione is used as an active ingredient in the development of new pesticides or herbicides. Its unique molecular structure may provide novel modes of action and selectivity for controlling pests and weeds.
Used in Material Science:
(3aR,6Z,9R,10aS,11aS)-2,3,3a,10,10a,11a-Hexahydro-3,3,6,9,11a-pentamethyl-1H-dicyclopenta[a,d]cyclononene-1,5,11(4H,9H)-trione is utilized in material science for the creation of new materials with specific properties. Its molecular structure and functional groups can be leveraged to develop materials with tailored characteristics for various applications, such as high-performance polymers or advanced coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 58298-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,9 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58298-76:
(7*5)+(6*8)+(5*2)+(4*9)+(3*8)+(2*7)+(1*6)=173
173 % 10 = 3
So 58298-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C20H26O3/c1-11-6-13-8-12(2)15(21)9-16-19(3,4)10-17(22)20(16,5)18(23)14(13)7-11/h6,8,11,14,16H,7,9-10H2,1-5H3/b12-8-/t11?,14-,16+,20-/m0/s1
58298-76-3Relevant articles and documents
Concise total syntheses of the bioactive mesotricyclic diterpenoids jatrophatrione and citlalitrione
Yang, Jiong,Long, Yun Oliver,Paquette, Leo A.
, p. 1567 - 1574 (2003)
The highly functionalized [5.9.5] tricyclic framework resident in jatrophatrione (1) and citlalitrione (2) has been synthesized. The route begins with the tandem anionic oxy-Cope rearrangement/methylation/transannular ene cyclization of 21 and subsequent introduction of a conjugated enone double bond. Hydroxyl-directed 1,4-reduction of this functionality in 25 with LiAlH4/Cul/hexamethylphosphoramide/tetrahydrofuran sets the stage for the implementation of a Grob fragmentation and expedited generation of 27. Stereocontrolled intramolecular hydrosilylation allows for the subsequent introduction of a cyclic carbonate as in 53. This intermediate undergoes remarkably efficient, fully regiocontrolled Treibs reaction to generate 54, with this maneuver serving as a pivotal step for making 1 available five steps later. Treatment of 1 with m-chloroperbenzoic acid leads to 2, with attack occurring preferentially on a α-face of the double bond more remote to the carbonyl.
