626-06-2

Usage

Uses

Used in Pharmaceutical Industry:
2,6-Dihydroxypyridine is used as a precursor for the production of various pharmaceutical drugs. Its ability to chelate metal ions and act as a ligand in coordination complexes makes it a valuable component in the synthesis of drug molecules with specific therapeutic properties.
Used in Agricultural Chemical Industry:
2,6-Dihydroxypyridine is used as a precursor for the production of agricultural chemicals. Its chelating and ligand properties contribute to the development of effective agrochemicals with targeted applications in crop protection and enhancement.
Used in Coordination Chemistry:
2,6-Dihydroxypyridine is used as a ligand in the development of coordination complexes. Its ability to bind to metal ions allows for the creation of stable complexes with unique properties, which can be utilized in various chemical reactions and applications.
Used in Catalyst Development:
2,6-Dihydroxypyridine is used as a ligand in the development of catalysts for chemical reactions. Its chelating properties enable the formation of active sites on metal ions, enhancing the efficiency and selectivity of catalytic processes.
Used in Antioxidant Applications:
2,6-Dihydroxypyridine is used as an antioxidant in the development of new materials for industrial and medical applications. Its ability to neutralize reactive oxygen species and protect against oxidative damage makes it a promising candidate for applications in material science and healthcare.

InChI:InChI=1/C5H5NO2/c7-4-2-1-3-5(8)6-4/h1-3H,(H2,6,7,8)

Upstream product

• 141-86-6 2.6-diaminopyridine 
• 13472-57-6 2,6-bis(ethoxy)pyridine 
• 237758-28-0 2,6-dihydroxy-pyridine-3,5-dicarboxylic acid diethyl ester 
• 7664-93-9 sulfuric acid 
• 140693-18-1 6-amino-pyridin-2-ol; sulfate 
• 6231-18-1 2,6-dimethoxypyridine 
• 7732-18-5 water 

Downstream Products

• 97431-93-1 2,2'-<2,6-pyridinediylbis(oxy-2,1-ethanediyloxy)>diphenyl dibenzyl ether 
• 97432-00-3 C₂₁H₂₁NO₆ 
• 1174281-33-4 6-hydroxy-1-tosylpyridin-2(1H)-one 
• 1174281-23-2 pyridine-2,6-diyl bis(4-methylbenzenesulfonate) 
• 946128-73-0 dimethylcarbamic acid 3-(3-(methylaminosulfonyl)aminobenzyl)-4-methyl-2-oxo-2H-pyrano[2,3-b]pyridin-7-yl ester 
• 946125-72-0 dimethylcarbamic acid 3-(3-aminobenzyl)-4-methyl-2-oxo-2H-pyrano[2,3-b]pyridin-7-yl ester 
• 946132-31-6 dimethyl-carbamic acid 4-methyl-3-(3-nitrobenzyl)-2-oxo-2H-pyrano[2,3-b]pyridin-7-yl ester 
• 1298016-44-0 C₂₁H₉N₅O₂ 
• 946125-89-9 7-hydroxy-4-methyl-3-(3-nitrobenzyl)-pyrano[2,3-b]pyridin-2-one 
• 120482-93-1 3,4-dimethyl-7-(2'-oxocyclohexyloxy)pyrano<2,3-b>pyridin-2-one 
• 120482-98-6 3,4,4'-trimethyl-8-azapsoralen 
• 120482-99-7 3,4,4',5'-tetramethylazapsoralen 

Relevant academic research and scientific papers

Process for preparation of polyhydric alcohols

A process for preparing a polyhydric alcohol according to the invention comprises subjecting a polyhydric alcohol compound having protected hydroxy group(s) to microwave irradiation in the presence of basic compound(s) or acid(s) having an acid dissociation exponent (pKa) of ?8 to 3 at 25° C. to remove the protecting groups of the hydroxy group of the polyhydric alcohol compound. The invention can provide an industrially advantageous process for preparing polyhydric alcohols by readily removing protecting group(s) from protected hydroxy group(s) of polyhydric alcohol compounds.

Water soluble cationic azo dyestuffs containing a cyclammonium group

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.