ChemicalBook Product Catalog Pharmaceutical intermediates Heterocyclic compound Pyridine compound Pyridine derivatives 3-Methoxy-2-methyl-1H-pyridin-4-one

3-Methoxy-2-methyl-1H-pyridin-4-one

3-Methoxy-2-methyl-1H-pyridin-4-one Basic information
Product Name:3-Methoxy-2-methyl-1H-pyridin-4-one
Synonyms:3-METHOXY-2-METHYL-1H-PYRIDIN-4-ONE 97;3-Methoxy-2-methyl-4(1H)-pyridinone;2-Methyl-3-methoxypyridine-4-one;3-Methoxy-2-methyl-1H-pyridin-4-one;3-methoxy-2-methyl-4-pyridone;4-Pyridinol, 3-methoxy-2-methyl-;3-methoxy-2-methyl-1,4-dihydropyridin-4-one;3-Methoxy-2-methyl-1H-pyridin-4-one
CAS:76015-11-7
MF:C7H9NO2
MW:139.15
EINECS:616-282-9
Product Categories:C7 and C8;Heterocyclic Building Blocks;Pyridines, Pyrimidines, Purines and Pteredines;Pyridines
Mol File:76015-11-7.mol
3-Methoxy-2-methyl-1H-pyridin-4-one Structure
3-Methoxy-2-methyl-1H-pyridin-4-one Chemical Properties
Melting point 156-160 °C (lit.)
Boiling point 252.7±40.0 °C(Predicted)
density 1.12±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka11.07±0.69(Predicted)
color Beige
InChIKeyGNWSQENQZGWCSW-UHFFFAOYSA-N
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 2933399990
MSDS Information
3-Methoxy-2-methyl-1H-pyridin-4-one Usage And Synthesis
Uses3-Methoxy-2-methylpyridin-4(1H)-one has been used as a reactant for the synthesis of 4-pyridone nucleoside derivatives as potential antitumor agents.
3-([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]OXY)-2-METHYL-4(1H)-PYRIDINONE Methyl 3-[(2-CHLORO-6-FLUOROBENZYL)OXY]-1-(2,4-DICHLOROBENZYL)-2-METHYL-4(1H)-PYRIDINONE 3-[(2-CHLORO-6-FLUOROBENZYL)OXY]-1-(4-FLUOROBENZYL)-2-METHYL-4(1H)-PYRIDINONE 3-[(2-CHLORO-6-FLUOROBENZYL)OXY]-2-METHYL-4(1H)-PYRIDINONE 3-Methoxy-2-methyl-1H-pyridin-4-one 5-BROMO-3-([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]OXY)-2-METHYL-4(1H)-PYRIDINONE Methoxy 3-[(2-CHLORO-6-FLUOROBENZYL)OXY]-2-METHYL-1-(4-NITROBENZYL)-4(1H)-PYRIDINONE Kresoxim-methyl 3-[(4-CHLOROBENZYL)OXY]-1-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]-2-METHYL-4(1H)-PYRIDINONE 1-[3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]-3-([3-CHLORO-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]OXY)-2-METHYL-4(1H)-PYRIDINONE 3-[(2-CHLORO-6-FLUOROBENZYL)OXY]-2-METHYL-1-(3-NITRO-2-PYRIDINYL)-4(1H)-PYRIDINONE 1-(2-CHLORO-6-FLUOROBENZYL)-3-[(2-CHLORO-6-FLUOROBENZYL)OXY]-2-METHYL-4(1H)-PYRIDINONE 3-[(2,6-DICHLOROBENZYL)OXY]-2-METHYL-4(1H)-PYRIDINONE 3-[(4-CHLOROBENZYL)OXY]-2-METHYL-4(1H)-PYRIDINONE 3-[(2-CHLORO-6-FLUOROBENZYL)OXY]-2-METHYL-1-(4-METHYLBENZYL)-4(1H)-PYRIDINONE 1-(4-CHLOROBENZYL)-3-[(2-CHLORO-6-FLUOROBENZYL)OXY]-2-METHYL-4(1H)-PYRIDINONE
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