24079-73-0 Usage
General Description
2,4,5-Trinitroimidazole (TNI) is a highly explosive and sensitive chemical compound used primarily for military and industrial applications. It is a nitro-substituted derivative of imidazole and is known for its high energy content and stability. TNI is a yellow crystalline solid with a molecular formula of C3H3N5O6 and a molecular weight of 209.09 g/mol. It is used as a component in explosive formulations and propellants due to its high detonation velocity and brisance. TNI has also been studied for its potential use as a high-energy density material for advanced energetic applications. However, its extreme sensitivity and explosive nature warrant 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 articles and documents
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.
