24079-73-0 Usage
Uses
Used in Military Applications:
2,4,5-Trinitroimidazole is used as an explosive component in military applications for its high detonation velocity and brisance, making it suitable for use in explosive formulations and propellants.
Used in Industrial Applications:
In the industrial sector, 2,4,5-Trinitroimidazole is utilized as a high-energy density material for advanced energetic applications, contributing to the development of more powerful and efficient systems.
Used in Research and Development:
2,4,5-Trinitroimidazole is also used as a subject of research for its potential applications in various fields, given its unique properties. However, due to its extreme sensitivity and explosive nature, it requires careful handling and storage to prevent accidental detonation.
Check Digit Verification of cas no
The CAS Registry Mumber 24079-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,7 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24079-73:
(7*2)+(6*4)+(5*0)+(4*7)+(3*9)+(2*7)+(1*3)=110
110 % 10 = 0
So 24079-73-0 is a valid CAS Registry Number.
InChI:InChI=1/C3HN5O6/c9-6(10)1-2(7(11)12)5-3(4-1)8(13)14/h(H,4,5)
24079-73-0Relevant academic research and scientific papers
Thermal Rearrangement of 1,4-Dinitroimidazole to 2,4-Dinitroimidazole: Characterization and Investigation of the Mechanism by Mass Spectrometry and Isotope Labeling
Bulusu, S.,Damavarapu, R.,Autera, J. R.,Behrens, R., Jr.,Minier, L. M.,et al.
, p. 5009 - 5015 (2007/10/02)
The thermal rearrangement of 1,4-dinitroimidazole to 2,4-dinitroimidazole has been investigated by differential scanning calorimetry and mass spectrometry techniques.When mixtures of independently prepared deuterium- and (15)N-labeled samples of the 1,4-isomer were subjected to thermal rearrangement, the resulting 2,4-dinitroimidazole failed to show isotope-scrambled molecular ions in its mass spectrum, suggesting that the reaction was intramolecular in nature.This was interpreted to mean that the mechanism was of the (1,5)-sigmatropic type rearrangement.Extensive NMR measurements were used to obtain unequivocal evidence for the identity of the assumed structures of the isomeric dinitroimidazoles.Two byproducts (4-nitroimidazole and a trinitroimidazole), formed during the rearrangement reaction, have also been identified.Plausible mechanisms for their formation are discussed.
