34892-82-5 Usage
Chemical composition
1,3,5-trinitrobenzene (TNB) is a benzene ring with three nitro groups (-NO2) attached at the 1, 3, and 5 positions; Tetraphene is a large polycyclic aromatic hydrocarbon molecule composed of four fused benzene rings.
Potential applications
The mixture has potential applications in the field of energetic materials and explosives.
Properties
The resulting compound may exhibit high thermal stability, energy density, and insensitivity to mechanical stimuli.
Suitability
Due to its properties, the compound is suitable for use in military and industrial applications.
New chemical properties
The combination of 1,3,5-trinitrobenzene and tetraphene may lead to the formation of new chemical properties and behavior.
Research interest
The new properties and behavior of the compound could be of interest for scientific research and practical use.
Check Digit Verification of cas no
The CAS Registry Mumber 34892-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34892-82:
(7*3)+(6*4)+(5*8)+(4*9)+(3*2)+(2*8)+(1*2)=145
145 % 10 = 5
So 34892-82-5 is a valid CAS Registry Number.
34892-82-5Relevant academic research and scientific papers
ELECTRON-ATTRACTING PROPERTIES OF FUNCTIONALIZED TRINITROBENZENES: SPECTROSCOPIC AND CALORIMETRIC STUDY OF CRYSTALLINE COMPLEXES WITH POLYNUCLEAR AROMATIC HYDROCARBONS
Casellato, Fulvia,Mascherpa, Achille,Turrio, Luigi,Girelli, Alberto
, p. 587 - 592 (2007/10/02)
The variation of the electron-accepting capability of functionalized trinitrobenzenes with changing functional group has been studied.The formation of charge-transfer complexes with polynuclear aromatic hydrocarbons appears to be affected more by steric hindrance of the functional groups than by their electron-withdrawing properties.The CT values of substituted trinitrobenzene-polynuclear aromatic hydrocarbon complexes is neither correlable with the electronic properties of functional groups nor with the Hammett ?p parameter.
