1600-31-3

Usage

InChI:InChI=1/C6H3N6O6/c7-9-8-6-4(11(15)16)1-3(10(13)14)2-5(6)12(17)18/h1-2,7H/q+1

Upstream product

• 88-88-0 2,4,6-trinitrochlorobenzene 
• 88-74-4 2-nitro-aniline 
• 88-89-1 2,4,6-Trinitrophenol 
• 1516-58-1 o-azidonitrobenzene 

Downstream Products

• 606-35-9 1-methoxy-2,4,6-trinitrobenzene 
• 2919-12-2 trinitro-2,4,6 diphenylamine 
• 17683-29-3 cyclooctylidene-2,4,6-trinitroaniline 
• 76569-24-9 Bis-(2,3-dihydro-1H-pyrrolo[1,2-a]indol-9-yl)-diazene; compound with 2,4,6-trinitro-phenylamine 
• 126822-11-5 C₁₄H₁₈N₁₀O₆ 
• 96694-50-7 2,2,3,3,5,7,9,9,10,10-Decamethyl-6,12-bis-(2,4,6-trinitro-phenyl)-1,4,8,11-tetraoxa-6,12-diaza-5λ⁵,7λ⁵-diarsa-dispiro[4.1.4.1]dodecane 
• 141461-62-3 6'-bicyclo<3.2.2>nonylidene-2,4,6-trinitroaniline 
• 141461-63-4 Bicyclo[4.2.1]non-(2E)-ylidene-(2,4,6-trinitro-phenyl)-amine 
• 141461-61-2 (1-bicyclo<3.2.1>octylmethylidene)-2,4,6-trinitroaniline 
• 96694-40-5 2,6,8,10,12,16-Hexamethyl-9,18-bis-(2,4,6-trinitro-phenyl)-1,7,11,17-tetraoxa-4,9,14,18-tetraaza-8λ⁵,10λ⁵-diarsa-dispiro[7.1.7.1]octadecane 
• 54948-87-7 P,P,P-triphenyl-N-(trinitrophenyl)phosphine imide 
• 96694-48-3 (2-Chloro-2λ⁵-benzo[1,3,2]dioxarsol-2-ylidene)-(2,4,6-trinitro-phenyl)-amine 
• 17683-30-6 1-Methyl-2-pikrylimino-cyclopentan 
• 17683-28-2 N-Pikrylimino-cycloheptan 

Relevant academic research and scientific papers

Thermal behavior, decomposition mechanism and thermal safety of 5,7-diamino-4,6-dinitrobenzenfuroxan (CL-14)

Thermal decomposition kinetics and mechanism of the high-energetic material 5,7-diamino-4,6-dinitrobenzenfuroxan (CL-14) were determined by differential scanning calorimetry (DSC), rapid scanning Fourier transform infrared spectroscopy, and simultaneous thermogravimetric and DSC analyses, coupled with FT-IR and mass spectroscopy. To evaluate the thermal safety of 5,7-diamino-4,6-dinitrobenzenfuroxan (CL-14), its specific heat capacity (Cp) was measured by DSC, and thermal conductivity (λ) was estimated. Kinetic parameters and heat of exothermic decomposition reaction of CL-14 were obtained by analysis of DSC curves. Kinetic parameters used to evaluate the thermal safety of CL-14, such as self-accelerating decomposition temperature (TSADT), critical temperature of thermal explosion (Tb) and impact sensitivity (H50), were obtained. Results showed that for CL-14, TSADT?=?282.0?°C and Tb?=?307.9?°C, whereas H50?=?39.79?cm, revealing that CL-14 had better thermal safety and heat resistance than HMX, RDX and GNTO.

The activation of SNAr reactions by the superstrong electron-withdrawing substituent CF3S(O)=NSO2CF3

The chlorine lability of the 2-nitrochlorobenzene derivative which contains the superstrong electron-withdrawing substituent CF3S(O)=NSO2CF3 in position 4 has been compared with the analogous 4-trifluoromethylsulphonyl derivative and picryl chloride in nucleophilic substitution.During interaction with hard nucleophilic agents, the effect of one superstrong substituent approximately corresponds to the influence of two nitro groups in positions 2 and 4.With soft reagents, picryl chloride is more active than the compound containing the CF3S(O)=NSO2CF3 group, polarizable only with difficulty.

Influence of strain on chemical reactivity. Relative reactivity of torsionally strained double bonds in 1,3-dipolar cycloadditions

The addition of picryl azide to a series of mono- and bicyclic olefins including trans- cycloalkenes and bridgehead alkenes is reported. Secondary reaction products were identified, and their mechanism of formation was explained by an analysis relating th