14916-60-0 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
2,3-Dinitropyridine is used as a precursor in the synthesis of various pharmaceuticals and agrochemicals for its ability to contribute to the development of new compounds with desired properties.
Used in Dye and Pigment Industries:
2,3-Dinitropyridine is used as a starting material in the manufacture of dyes and pigments, enabling the production of a wide range of colorants for various applications.
Used in Specialty Chemicals Industry:
2,3-Dinitropyridine is used as a building block in the synthesis of specialty chemicals, contributing to the development of unique products with specific functionalities.
Used in Materials Science:
2,3-Dinitropyridine is used in the field of materials science for its potential application in the development of energetic materials and propellants, due to its explosive nature and reactivity.
Used in Research and Development:
2,3-Dinitropyridine is used in research and development settings for studying its properties and exploring its potential applications in various fields, including pharmaceuticals, agrochemicals, dyes, pigments, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 14916-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,1 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14916-60:
(7*1)+(6*4)+(5*9)+(4*1)+(3*6)+(2*6)+(1*0)=110
110 % 10 = 0
So 14916-60-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H3N3O4/c9-7(10)4-2-1-3-6-5(4)8(11)12/h1-3H
14916-60-0Relevant academic research and scientific papers
Tetrazolopyridines and Furazanopyridine 1-Oxides
Lowe-Ma, Charlotte K.,Nissan, Robin A.,Wilson, William S.
, p. 3755 - 3761 (2007/10/02)
Tetrazolopyridines may be prepared by the reaction of azide ion with 2-chloropyridines.These tetrazolopyridines are shown to be in equilibrium with the corresponding 2-azidopyridines.Furazanopyridine 1-oxides may be prepared by thermolysis of the appropriate 4-nitrotetrazolopyridines, presumably via the corresponding 2-azido-3-nitropyridines.The furazanopyridine 1-oxides are found to be in equilibrium with the 3-oxides. 1H and 13C NMR are used to examine this equilibrium.
