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Details

Stereochemistry ACHIRAL
Molecular Formula C6H7NO
Molecular Weight 109.1259
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-METHYL-2-PYRIDONE

SMILES

CC1=CC=CNC1=O

InChI

InChIKey=MVKDNXIKAWKCCS-UHFFFAOYSA-N
InChI=1S/C6H7NO/c1-5-3-2-4-7-6(5)8/h2-4H,1H3,(H,7,8)

HIDE SMILES / InChI

Molecular Formula C6H7NO
Molecular Weight 109.1259
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and phytotoxic activity of new pyridones derived from 4-hydroxy-6-methylpyridin-2(1H)-one.
2009-12-01
Origin of methyl torsional barrier in 1-methyl-2(1H)-pyridinimine and 3-methyl-2(1H)-pyridone: II. Ground state.
2007-03-21
Spectroscopic studies on methyl torsional behavior in 1-methyl-2(1H)-pyridone, 1-methyl-2(1H)-pyridinimine, and 3-methyl-2(1H)-pyridone. I. Excited state.
2007-03-21
Polaronic semiconductor behavior of long-range charge transfer in DNA oligomers in solution: controlling barriers to long-distance radical cation migration in DNA with thymine analogs.
2006
Synthesis of a dA-dT base pair analogue and its effects on DNA-ligand binding.
2001-08
Minor groove functional groups are critical for the B-form conformation of duplex DNA.
2001-01-30
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:49:18 GMT 2025
Edited
by admin
on Mon Mar 31 19:49:18 GMT 2025
Record UNII
VM19FN4HHV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-METHYL-2-PYRIDONE
Systematic Name English
NSC-4343
Preferred Name English
Code System Code Type Description
ECHA (EC/EINECS)
213-710-2
Created by admin on Mon Mar 31 19:49:18 GMT 2025 , Edited by admin on Mon Mar 31 19:49:18 GMT 2025
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EPA CompTox
DTXSID50143118
Created by admin on Mon Mar 31 19:49:18 GMT 2025 , Edited by admin on Mon Mar 31 19:49:18 GMT 2025
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MESH
C506007
Created by admin on Mon Mar 31 19:49:18 GMT 2025 , Edited by admin on Mon Mar 31 19:49:18 GMT 2025
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PUBCHEM
70481
Created by admin on Mon Mar 31 19:49:18 GMT 2025 , Edited by admin on Mon Mar 31 19:49:18 GMT 2025
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CAS
1003-56-1
Created by admin on Mon Mar 31 19:49:18 GMT 2025 , Edited by admin on Mon Mar 31 19:49:18 GMT 2025
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FDA UNII
VM19FN4HHV
Created by admin on Mon Mar 31 19:49:18 GMT 2025 , Edited by admin on Mon Mar 31 19:49:18 GMT 2025
PRIMARY
NSC
4343
Created by admin on Mon Mar 31 19:49:18 GMT 2025 , Edited by admin on Mon Mar 31 19:49:18 GMT 2025
PRIMARY