364594-08-1 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-(3-hydroperoxycyclohexyl)(9CI) is utilized as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable component in the creation of complex organic molecules.
Used in Chemical Reactions as a Reagent:
Due to its reactive hydroperoxycyclohexyl group, Ethanone, 1-(3-hydroperoxycyclohexyl)(9CI) serves as a reagent in a range of chemical reactions. It can facilitate the formation of new chemical bonds and aid in the synthesis of target molecules, contributing to the advancement of chemical research and development.
Used in Pharmaceutical Industry:
Ethanone, 1-(3-hydroperoxycyclohexyl)(9CI) may be employed as a building block in the development of pharmaceutical compounds. Its unique structure could be leveraged to create novel drugs with specific therapeutic properties, pending further research into its bioactivity and pharmacological potential.
Used in Research and Development:
In the field of scientific research, Ethanone, 1-(3-hydroperoxycyclohexyl)(9CI) is used as a subject of study to explore its chemical properties, reactivity, and potential applications. Understanding its behavior in various chemical environments can lead to new insights and innovations in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 364594-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,4,5,9 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 364594-08:
(8*3)+(7*6)+(6*4)+(5*5)+(4*9)+(3*4)+(2*0)+(1*8)=171
171 % 10 = 1
So 364594-08-1 is a valid CAS Registry Number.
364594-08-1Relevant academic research and scientific papers
Yingzhaosu A analogues: Synthesis by the ozonolysis of unsaturated hydroperoxides, structural analysis and determination of anti-malarial activity
Tokuyasu, Takahiro,Masuyama, Araki,Nojima, Masatomo,McCullough, Kevin J,Kim, Hye-Sook,Wataya, Yusuke
, p. 5979 - 5989 (2007/10/03)
Ozone-mediated cyclization of a series of unsaturated hydroperoxides 7, prepared from dienes 2, afforded the corresponding yingzhaosu A analogues 9 in moderate to high yield. X-Ray crystallographic analysis of two yingzhaosu A analogues, endo-9f and 13, showed that the 2,3-dioxabicyclo[3.3.1]nonane system adopts a chair-boat arrangement. Subsequent treatment of endoperoxides 9 with Ag2O/MeI afforded the expected methyldioxy-substituted cyclic peroxides 14, several of which showed notable anti-malarial activity against P. falciparum in vitro.
