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3,5-diethyl-1,2,4-trioxolane is a cyclic ether compound with the molecular formula C6H12O3. It is characterized by two ethyl groups (C2H5) attached to the 3rd and 5th carbon atoms of the 1,2,4-trioxolane ring, which consists of three oxygen atoms and one carbon atom. This chemical is known for its unique properties, such as its ability to form peroxides and its potential use as a solvent or intermediate in the synthesis of other organic compounds. Due to its reactivity, it is important to handle 3,5-diethyl-1,2,4-trioxolane with care, as it can be sensitive to heat, light, and friction, which may lead to the formation of hazardous peroxides.

873-72-3

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873-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 873-72-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 873-72:
(5*8)+(4*7)+(3*3)+(2*7)+(1*2)=93
93 % 10 = 3
So 873-72-3 is a valid CAS Registry Number.

873-72-3Downstream Products

873-72-3Relevant articles and documents

Formation of secondary ozonides in the gas phase low-temperature ozonation of primary and secondary alkenes

Fajgar, Radek,Vitek, Josef,Haas, Yehuda,Pola, Josef

, p. 239 - 248 (2007/10/03)

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.

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