25243-36-1 Usage
Highly explosive compound
Due to its powerful oxidizing properties, it is commonly used in the production of explosives and propellants.
Sensitivity to heat, shock, and friction
It is prone to accidental detonation, making it extremely sensitive to these factors.
Strictly regulated and controlled
Its use is strictly regulated and controlled due to its potential for harm if mishandled.
High energy yield
Known for its high energy yield, making it an important ingredient in military and industrial applications.
Careful handling and storage
Requires careful handling and storage to prevent accidents and ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 25243-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,4 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25243-36:
(7*2)+(6*5)+(5*2)+(4*4)+(3*3)+(2*3)+(1*6)=91
91 % 10 = 1
So 25243-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H4N8O8/c21-17(22)5-1-7-11(9(3-5)19(25)26)13-16-8-2-6(18(23)24)4-10(20(27)28)12(8)14-15(7)16/h1-4H
25243-36-1Relevant articles and documents
Reactions of benzotriazolo[2,1-a]benzotriazole derivatives. 1. Synthesis of new insensitive high-density energetic compounds
Subramanian,Boyer,Buzatu,Stevens,Trudell
, p. 6110 - 6113 (2007/10/03)
The sequential preference of electrophilic attack on the dibenzotetraazapentalene ring system 6 has unequivocally been shown to be in the order of position 2(8) > 4(10) >> 1(7) and 3(9). However, nucleophilic substitution reactions with sodium azide were found to be substrate dependent. Substitution occurred at the 3(9)-position of 9 followed by elimination of hydrogen chloride to give 10 while direct substitution of azide for the 4(10)-nitro group of 2 was found to yield 13. The reactivity of the dibenzotetraazapentalene derivatives toward electrophiles and nucleophiles was exploited for the synthesis of the new heterocyclic system 14H-[1,2,5]oxadiazolo[3,4-e][1,2,5]-oxadiazolo[3',4':4,5]benzotriazolo [2,1-a]benzotriazol-6-ium inner salt 1,8-dioxide (11). From this study the first of a new class of insensitive energetic materials 4 has been synthesized in a straightforward fashion from 2.