14533-64-3 Usage
Uses
Used in Pharmaceutical Industry:
2,6-Dihydroxypyridine-4-carboxamide is used as a key intermediate in the synthesis of various pharmaceuticals for its versatile chemical properties and potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2,6-Dihydroxypyridine-4-carboxamide is utilized as a building block for the development of new agrochemicals, contributing to crop protection and enhancement of agricultural yields.
Used in Dye and Pigment Industry:
2,6-Dihydroxypyridine-4-carboxamide is employed as a precursor in the manufacturing of dyestuffs and pigments, leveraging its chemical structure to produce a range of colorants for various applications.
Used in Cancer Treatment Research:
2,6-Dihydroxypyridine-4-carboxamide and its derivatives are studied for their potential as anticancer agents, targeting various types of cancer through different mechanisms of action.
Used in Viral Infection Treatment Research:
2,6-Dihydroxypyridine-4-carboxaMide is also explored for its potential in treating viral infections, with research focusing on its antiviral properties and possible applications in medicine.
Used in Neurodegenerative Disease Treatment Research:
2,6-Dihydroxypyridine-4-carboxamide is under investigation for its possible role in the treatment of neurodegenerative diseases, with studies examining its effects on neurological conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 14533-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,3 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14533-64:
(7*1)+(6*4)+(5*5)+(4*3)+(3*3)+(2*6)+(1*4)=93
93 % 10 = 3
So 14533-64-3 is a valid CAS Registry Number.
14533-64-3Relevant academic research and scientific papers
Water soluble cationic azo dyestuffs containing a cyclammonium group
-
, (2008/06/13)
A mixture of water soluble cationic azo dyestuffs devoid of carboxylic acid or sulphonic acid groups, each dyestuff in said mixture containing at least one cyclammonium group and said dyestuffs differing only in the constitution of the said cyclammonium group, said cyclammonium group being a gamma-picolinium group in one dyestuff and a beta-picolinium group in another dyestuff in said mixture, the water-solubility of said mixture being superior to that of the individual dyestuffs, the mixture being particularly useful for the coloration of polymers and copolymers of acrylonitrile.