770-50-3 Usage
Chemical class
1,2,4-trioxolanes A class of organic compounds that contain a six-membered ring with three oxygen atoms.
Structure
Cyclic peroxide compound Contains a six-membered ring with three oxygen atoms and a hexyl group attached.
Functional group
Hexyl group A six-carbon alkyl chain that is attached to the cyclic peroxide ring.
Application
Antimalarial drugs Used in the development of antimalarial drugs due to its ability to release reactive oxygen species in acidic environments.
Antimalarial activity
Promising Has shown promising antimalarial activity, making it a potential candidate for the treatment and prevention of malaria.
Additional application
Cancer treatment Has been studied for its potential application in cancer treatment.
Mechanism of action
Induces selective cell death Can induce selective cell death in cancer cells, making it a potential candidate for cancer treatment.
Reactivity
Reactive oxygen species Capable of releasing reactive oxygen species in acidic environments, which contributes to its antimalarial and potential anticancer properties.
Check Digit Verification of cas no
The CAS Registry Mumber 770-50-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,7 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 770-50:
(5*7)+(4*7)+(3*0)+(2*5)+(1*0)=73
73 % 10 = 3
So 770-50-3 is a valid CAS Registry Number.
770-50-3Relevant academic research and scientific papers
Fajgar, Radek,Vitek, Josef,Haas, Yehuda,Pola, Josef
, p. 239 - 248 (1999)
The gas-phase ozonation of a series of alkenes RCH=CH2 (R = Et, Hex), trans-RHC=CHR (R = Me, Et, Pri) and Me2C=CMe2 at -40 to 20°C, and that of ethene H2C=CH2 at -120 to 0°C at 10-4 v/v concentrations in N2 at atmospheric pressure have been studied. Using complementary product analysis by means of GC-FTIR and GC-MS techniques, we present conclusive evidence for the formation of secondary alkene ozonides as high-yield products in all instances except Me2C=CMe2. It is shown that the stereoselectivity for the conversion of trans-RHC=CHR (R = Me, Et, Pri) to trans-secondary ozonides in the gas phase is similar to that observed earlier in solution, and that the yields of secondary ozonides from RHC=CH2, but not those from RHC=CHR, significantly decrease with increasing temperature.
