5407-93-2 Usage
Uses
Used in Pharmaceutical Industry:
2-hydroxy-4,6-dimethyl-5-nitronicotinonitrile is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-hydroxy-4,6-dimethyl-5-nitronicotinonitrile serves as an intermediate in the production of agrochemicals, aiding in the creation of compounds that can be used in agriculture for pest control and crop protection.
Used in Research and Development:
2-hydroxy-4,6-dimethyl-5-nitronicotinonitrile is utilized in research and development for the exploration and creation of new compounds. Its unique properties make it a valuable asset in scientific studies aimed at discovering novel applications and enhancing existing ones.
Used in Organic Chemistry:
2-hydroxy-4,6-dimethyl-5-nitronicotinonitrile plays a role in the field of organic chemistry, where it can be used to synthesize a variety of organic compounds, contributing to the advancement of chemical knowledge and the development of new chemical processes.
Used in Material Science:
2-hydroxy-4,6-dimethyl-5-nitronicotinonitrile also has potential applications in material science, where it may be employed in the design and synthesis of new materials with specific properties for use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5407-93-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5407-93:
(6*5)+(5*4)+(4*0)+(3*7)+(2*9)+(1*3)=92
92 % 10 = 2
So 5407-93-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3O3/c1-4-6(3-9)8(12)10-5(2)7(4)11(13)14/h1-2H3,(H,10,12)
5407-93-2Relevant academic research and scientific papers
PYRIDYL COMPOUND SUITABLE FOR THE TREATMENT OF METABOLIC DISORDERS
-
Page/Page column 57, (2015/01/16)
The description relates to a pyridyl compound of Formula 1 wherein A, B, X, R1, R2, R3, R4, R5, R6, and n are as defined in the specification, in all their isotopic forms, stereoisomeric and tautomeric forms and mixtures thereof in all ratios, their pharmaceutically acceptable salts, N-oxides, pharmaceutically acceptable solvates, isosteres and prodrugs thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia. The description also relates to a process for the manufacture of the pyridyl compound and a pharmaceutical composition containing the pyridyl compound.
Synthesis of some halogen- and nitro-substituted nicotinic acids and their fragmentation under electron impact
Dyadyuchenko,Strelkov,Mikhailichenko,Zaplishny
, p. 308 - 314 (2007/10/03)
Features of electrophilic and nucleophilic substitution under chlorination and nitration reactions conditions have been investigated for 6-hydroxy- and 6-methyl-substituted derivatives of 3-cyano-4-methyl-2(1H)-pyridones. The polychloro- and nitro-substituted 3-cyano-4-methylpyridines obtained were used as synthons in the synthesis of some polyhalo- and nitro-substituted nicotinic acids and their amides. The fragmentation pathways of the synthesized compounds under electron impact have been studied.
