552424-65-4 Usage
Description
1(2H)-Pentalenone,3,3a,6,6a-tetrahydro-4,6a-dimethyl-,(3aR,6aS)-rel-(9CI) is a bicyclic chemical compound with a pentalenone core, which is naturally occurring in certain plants and fungi. It has been recognized for its potential bioactive properties and has been studied for its pharmacological activities, such as anti-inflammatory and antimicrobial effects. The unique structure and potential applications of this compound make it a subject of interest for further research and possible development as a pharmaceutical or agrochemical agent.
Uses
Used in Pharmaceutical Industry:
1(2H)-Pentalenone,3,3a,6,6a-tetrahydro-4,6a-dimethyl-,(3aR,6aS)-rel-(9CI) is used as a potential pharmaceutical agent due to its identified anti-inflammatory and antimicrobial activities. Its ability to modulate various biological pathways and exhibit bioactivity against certain pathogens makes it a promising candidate for the development of new drugs to treat inflammation and infections.
Used in Agrochemical Industry:
In the agrochemical industry, 1(2H)-Pentalenone,3,3a,6,6a-tetrahydro-4,6a-dimethyl-,(3aR,6aS)-rel-(9CI) is used as a potential agent for the development of new pesticides or fungicides. Its antimicrobial properties can be harnessed to protect crops from diseases caused by various microorganisms, thereby increasing crop yield and reducing the reliance on conventional chemical pesticides.
Check Digit Verification of cas no
The CAS Registry Mumber 552424-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,2,4,2 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 552424-65:
(8*5)+(7*5)+(6*2)+(5*4)+(4*2)+(3*4)+(2*6)+(1*5)=144
144 % 10 = 4
So 552424-65-4 is a valid CAS Registry Number.
552424-65-4Relevant articles and documents
Gold(I)-catalyzed cyclizations of silyl enol ethers: Application to the synthesis of (+)-lycopladine A
Staben, Steven T.,Kennedy-Smith, Joshua J.,Huang, David,Corkey, Britton K.,LaLonde, Rebecca L.,Toste, F. Dean
, p. 5991 - 5994 (2007/10/03)
(Chemical Equation Presented) In control: Gold(I)-catalyzed intramolecular addition of silyl enol ethers to alkynes and allenes allows for the diastereoselective synthesis of cyclopentenes with control of the position of the double bond. The utility of th