31163-68-5 Usage
General Description
2,6-dinitro-2H-indazole, also known as DNIZ, is a synthetic chemical compound that belongs to the class of indazoles. It is a powerful and potentially hazardous explosive material that is primarily used in military and industrial applications. DNIZ is highly sensitive to external stimuli such as heat, friction, and impact, making it extremely dangerous to handle and transport. Its explosive properties are a result of the presence of two nitro groups on the indazole ring, which contribute to its high energy content. Due to its potential for misuse and danger, DNIZ is strictly regulated and controlled in many countries, and its use is limited to authorized personnel and organizations.
Check Digit Verification of cas no
The CAS Registry Mumber 31163-68-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,6 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 31163-68:
(7*3)+(6*1)+(5*1)+(4*6)+(3*3)+(2*6)+(1*8)=85
85 % 10 = 5
So 31163-68-5 is a valid CAS Registry Number.
31163-68-5Relevant articles and documents
INDAZOLE DERIVATIVES USEFUL AS MELANIN CONCENTRATING RECEPTOR LIGANDS
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Page/Page column 51, (2008/12/05)
The present invention relates to novel compounds, in particular, novel indazole that may be used as melanin concentrating hormone receptor ligands, methods of preparing such compounds, compositions containing such compounds, and methods of using such compounds to treat MCH related disorders.
Azoles. Part 32: Nitroindazole derivatives and their electron affinity
Usarewicz,Wrzeciono,Lukaszewski,Gatniejewska,Peisert
, p. 15 - 18 (2007/10/02)
A modified procedure for the synthesis of the dinitroindazoles 5-8 is described. Treatment of the chloronitro- and dinitroindazoles 1-8 with epichlorohydrin afforded the chlorohydroxypropyl- and epoxypropylindazole derivatives 2a-8a, 1b-5b, 7b and 7c. The structure of the compounds is confirmed by the aid of their IR, 1H and 13C NMR spectra. The electron affinity of the nitroindazole derivatives 1-16 is discussed on the basis of their halfwave potentials and in the combination with their eventual radiosensitizing properties.