90222-68-7

Usage

Uses

Used in Pharmaceutical Industry:
(4-Hydroxy-6-methyl-2-oxo-2H-pyridin-1-yl)-acetic acid is used as a chelating agent for the synthesis of pharmaceuticals. Its ability to bind to metal ions allows for the creation of stable complexes, which can be beneficial in the development of new drugs and the improvement of existing ones.
Used in Agriculture:
In the agricultural industry, (4-Hydroxy-6-methyl-2-oxo-2H-pyridin-1-yl)-acetic acid is used as a metal chelator. This application helps to improve the bioavailability of essential nutrients for plants, thereby enhancing crop growth and yield.
Used in Food Industry:
(4-Hydroxy-6-methyl-2-oxo-2H-pyridin-1-yl)-acetic acid also finds use in the food industry as a preservative. Its chelating properties can help to extend the shelf life of various food products by preventing the oxidation and spoilage that can occur due to the presence of metal ions.
Used in Research and Development:
As a potential drug candidate, (4-Hydroxy-6-methyl-2-oxo-2H-pyridin-1-yl)-acetic acid is utilized in research and development for its biological activities. Scientists and researchers explore its potential applications in the treatment of various diseases and conditions, taking advantage of its unique chemical properties.

Upstream product

• 675-10-5 4-hydroxy-6-methyl-2-pyron 
• 56-40-6 glycine 

Downstream Products

• 130868-30-3 ethoxycarbonylmethylene-1 hydroxy-4 methyl-6 pyridone-2 
• 130868-37-0 bis(ethoxycarbonylmethylene-1 hydroxy-4 methyl-6 oxo-2 pyridinyl-3) 4-methoxyphenylmethane 
• 130887-34-2 bis(ethoxycarbonylmethylene-1 hydroxy-4 methyl-6 oxo-2 pyridinyl-3) 4-chlorophenylmethane 
• 130887-33-1 bis(ethoxycarbonylmethylene-1 hydroxy-4 methyl-6 oxo-2 pyridinyl-3)phenylmethane 
• 130868-35-8 ethoxycarbonylmethylene-1 hydroxy-4 methyl-6 (methoxy-4 α-piperidinobenzyl)-3 pyridone-2 
• 130868-36-9 ethoxycarbonylmethylene-1 hydroxy-4 methyl-6 (chloro-4 α-piperidinobenzyl)-3 pyridone-2 
• 130868-34-7 methoxycarbonylmethylene-1 hydroxy-4 methyl-6 (methoxy-4 α-piperidinobenzyl)-3 pyridone-2 
• 130868-33-6 ethoxycarbonylmethylene-1 hydroxy-4 methyl-6 (α-piperidinobenzyl)-3 pyridone-2 

Relevant academic research and scientific papers

Pyridone derivatives, their preparation and their use as synthesis intermediates

The invention concerns compounds of formula (I) in which: R is —NO2or —NHR3, R3being hydrogen, —COR4(R4selected among (C1-C4) alkyl, aryl and aryl (C1-C4) alkyl, —COOR5(R5selected among (C1-C4) alkyl and aryl (C1-C4) alkyl), —CONHR6or SO2R6(R6selected among (C1-C5) alkyl, aryl and aryl(C1-C4) alkyl), —SO2NR7R8(R7and R8independently of each other represent hydrogen or (C1-C4) alkyl or form with the nitrogen atom a morpholine group), aryl (C1-C4) alkyl, R1is a (C1-C4) alkyl group linear or branched, cyclo (C3-C8) alkyl, aryl optionally substituted, aryl (C1-C4) alkyl optionally substituted, heteroaryl, R2is a hydrogen atom, a (C1-C4) alkyl or arylmethyl group, X is an oxygen or sulphur atom, a —CH2—, —SO2or —NR1— group and Y is a hydrogen atom or (C1-C6) alkyl. The invention is applicable to synthesis intermediates.

MESOIONIC OXAZOLONES. VI. HYDROLYSIS OF ACYLATED DERIVATIVES

Nonplanar acylated mesoionic oxazolones 10-16 underwent hydrolysis at ambient temperature, while their planar analogs 8-9 did it only at 100 deg C. The same trend in reactivity was observed in the case of the monocyclic compounds 34a (planar) and 34b (non

Reactivite des esters de la carboxymethylene-1 hydroxy-4 methyl-6 pyridone-2 vis-a-vis des aldehydes aromatiques

A novel condensation of aromatic aldehyde with 2-pyridone: the 4-hydroxy-6-methyl-2-pyridone-1-acetate 1 and its esters 2 and 3 has been explored.It leads to the formation of arylmethanes 7 and 8 obtained by the reaction of one molecule of aldehyde with t