25065-00-3

Basic information

• Product Name: 1-Methyl-3-pyridone
• Synonyms: 1-Methyl-3-pyridone;3-Oxylato-1-methylpyridinium
• CAS NO: 25065-00-3
• Molecular Formula: C₆H₇NO
• Molecular Weight: 109.1259
• Mol File: 25065-00-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: 1-Methyl-3-pyridone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Methyl-3-pyridone(25065-00-3)
• EPA Substance Registry System: 1-Methyl-3-pyridone(25065-00-3)

Safety Data

• Hazardous Substances Data: 25065-00-3(Hazardous Substances Data)

Usage

Type

Chemical compound and derivative of pyridine

Uses

Synthesis of pharmaceuticals and agrochemicals

Biological activities

Antidiabetic, anti-inflammatory, and central nervous system effects

Inhibition

Potent inhibitor of aldehyde oxidase enzyme

Potential applications

Treatment of neurodegenerative diseases and cancer

Fields of use

Medicine, agriculture, and drug development.

InChI:InChI=1/C6H7NO/c1-7-4-2-3-6(8)5-7/h2-5H,1H3

Upstream product

• 109-00-2 3-HYDROXYPYRIDINE 
• 80-48-8 methyl p-toluene sulfonate 
• 7295-78-5 3-hydroxy-N-methylpyridinium chloride 
• 7500-05-2 3-hydroxy-1-methylpyridin-1-ium iodide 
• 4685-07-8 3-hydroxy-N-methylpyridinium ion 
• 74-88-4 methyl iodide 

Downstream Products

• 125217-79-0 N-methyl-6β-(phenylsulphonyl)-8-azabicyclo<3.2.1>oct-3-en-2-one 
• 125217-80-3 N-methyl-6α-fluoro-6β-(phenylsulphonyl)-8-azabicyclo<3.2.1>oct-3-en-2-one 
• 139730-35-1 N-methyl-(1R,5R,6S,R_S)-6-(p-tolylsulphinyl)-8-azabicyclo<3.2.1>oct-3-en-2-one 
• 139730-37-3 N-methyl-(1S,5S,6R,R_S)-6-(p-tolylsulphinyl)-8-azabicyclo<3.2.1>oct-3-en-2-one 
• 139730-38-4 N-methyl-(1R,5R,6R,R_S)-6-(p-tolylsulphinyl)-8-azabicyclo<3.2.1>oct-3-en-2-one 
• 139730-35-1 (1S,5S,6S)-8-Methyl-6-(toluene-4-sulfinyl)-8-aza-bicyclo[3.2.1]oct-3-en-2-one 
• 139730-35-1 (1R,5R,6S)-8-Methyl-6-(toluene-4-sulfinyl)-8-aza-bicyclo[3.2.1]oct-3-en-2-one 
• 139730-35-1 (1S,5S,6R)-8-Methyl-6-(toluene-4-sulfinyl)-8-aza-bicyclo[3.2.1]oct-3-en-2-one 
• 3554-74-3 3-Hydroxy-1-methylpiperidine 
• 125217-79-0 endo-6-benzenesulfonyl-8-methyl-8-azabicyclo<3.2.1>oct-3-en-2-one 
• 13466-55-2 tropan-2α-ol 
• 125217-76-7 N-methyl-(1S,5S,6R)-6-(p-tolylsulphenyl)-8-azabicyclo<3.2.1>octan-2-one 
• 125217-75-6 N-methyl-(1S,5S,6R)-6-(p-tolylsulphenyl)-8-azabicyclo<3.2.1>oct-3-en-2-one 
• 125217-77-8 N-methyl-(1S,2R,5S,6R)-6-(p-tolylsulphenyl)-8-azabicyclo<3.2.1>octan-2-ol 

Relevant articles and documents

On the preparation of some phospholipid analogues

Several structural analogues of the biocompatible diacyl glycerol phosphatidylcholine family have been prepared. Considerable variation in structure is allowed without impairing the desirable biocompatible properties. In particular, derivatives in which the fatty ester link is replaced by ether links and in which the central glycerol group is replaced by simple variants such as the symmetrical tris(hydroxymethyl)ethane group retain biocompatible properties. The Royal Society of Chemistry 2000.

Structure of the Calystegines: New alkaloids of the nortropane family

Three new alkaloids have been isolated from Calystegia sepium; their structures have been established from their 1H and 13C N.M.R. spectra, and confirmed by the synthesis of model compounds.