30192-58-6Relevant articles and documents
Energetic C-trinitromethyl-substituted pyrazoles: Synthesis and characterization
Zhang, Yiying,Li, Yanan,Hu, Jianjian,Ge, Zhongxue,Sun, Chenghui,Pang, Siping
, p. 1524 - 1529 (2019)
A new family of C-trinitromethyl-substituted pyrazoles was designed and obtained in good yields by the reaction of N2O4 with the pyrazolecarbaldehyde oxime followed by further N-nitration and C-nitration. All of the new compounds were fully characterized by IR and NMR spectroscopy, elemental analysis and differential scanning calorimetry (DSC). Compounds 2 and 3 were further confirmed by X-ray crystallography. These pyrazole derivatives have good densities, positive enthalpies of formation and acceptable sensitivity values. Theoretical calculations carried out using Gaussian 03 and EXPLO5 program demonstrate good to excellent detonation velocities and pressures in the range of ADN and HMX. Compound 3 exhibiting a positive oxygen balance, high specific impulse and moderate thermal stability is a promising high energy density oxidizer.
3-trinitromethylpyrazole compound
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Paragraph 0008; 0020-0024; 0028; 0040-0044; 0048, (2019/02/04)
The invention discloses a 3-trinitromethylpyrazole compound, which is of a structural formula as shown by a formula (I) as shown in the following descriptions. The 3-trinitromethylpyrazole compound ismainly used in the field of energetic materials.
Copper(ii)-promoted direct conversion of methylarenes into aromatic oximes
Yu, Jiatao,Lu, Ming
supporting information, p. 7397 - 7401 (2015/07/15)
A simple and efficient catalytic system for direct conversion of methylarenes into aromatic oximes has been developed, with Cu(OAc)2 as catalyst, NHPI (N-Hydroxyphthalimide) as additive, TBN (tert-butyl nitrite) as both the nitrogen source and the oxidant. This process proceeds under mild conditions, tolerates a wide range of substrates, affording the targeted aromatic oximes in 63-86% yields.