3101-79-9 Usage
Uses
Used in Chemical Research and Development:
Aniline 1,3,5-trinitrobenzene (1:1) is used as a research compound for studying the properties and reactions of highly toxic and explosive substances. Its unique combination of characteristics allows scientists to explore the behavior of such compounds under various conditions and develop methods for safe handling and disposal.
Used in Military and Defense Applications:
Due to its explosive properties, aniline 1,3,5-trinitrobenzene (1:1) may be utilized in the development of military and defense technologies, such as explosives and propellants. However, its use in these applications is highly regulated and restricted to ensure safety and prevent misuse.
Used in Industrial Applications with Strict Safety Protocols:
In certain industrial processes, aniline 1,3,5-trinitrobenzene (1:1) may be employed as a component in specific chemical reactions or as a catalyst. However, its use in these applications is limited to facilities with strict safety protocols and trained personnel to minimize the risk of accidents and ensure the safe handling of the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 3101-79-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,0 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3101-79:
(6*3)+(5*1)+(4*0)+(3*1)+(2*7)+(1*9)=49
49 % 10 = 9
So 3101-79-9 is a valid CAS Registry Number.
3101-79-9Relevant academic research and scientific papers
REACTION OF BIS(2,4,6-TRINITROPHENYL) SULFONE AND ITS DERIVATIVES WITH AMINES
Nurgatin, V. V.,Sharnin, G. P.,Nurgatina, R. B.,Ginzburg, B. M.
, p. 306 - 309 (2007/10/02)
The reaction of bis(2,4,6-trinitrophenyl) sulfone and some of its 3- and 3,3'-substituted derivatives with organic bases leads to the formation of an adduct of 1,3,5-trinitrobenzene or its substituted derivative and the respective amine, sulfur trioxide, and 2,4,6-trinitrodiphenylamine and its derivatives or derivatives of 2,4,6-trinitroaniline.The direction of reaction does not depend on the ratio of the initial compounds or on the temperature.It was established that attack by the nucleophilic reagent takes place at the ring in which the largest positive charge is induced at the carbon atom attached to the sulfur.
