U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO
Molecular Weight 121.1366
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-ACETYLPYRIDINE

SMILES

CC(=O)C1=CC=NC=C1

InChI

InChIKey=WMQUKDQWMMOHSA-UHFFFAOYSA-N
InChI=1S/C7H7NO/c1-6(9)7-2-4-8-5-3-7/h2-5H,1H3

HIDE SMILES / InChI

Molecular Formula C7H7NO
Molecular Weight 121.1366
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
4-Acetyl-pyridinium iodide.
2010-06-16
Hexa-kis-(4-acetyl-pyridinium) octa-deca-chloridotetra-anti-monate(III).
2010-06-05
Ruthenium(II)-arene complexes with functionalized pyridines: synthesis, characterization and cytotoxic activity.
2010-03
2-Methyl-2,4-di-4-pyridyl-2,3-dihydro-1H-1,5-benzodiazepine acetic acid solvate.
2009-11-25
4-Acetyl-pyridinium hydrogen sulfate.
2009-09-09
Two EE-azido-bridged nickel(II) layered compounds: vigorous twisted torsion angle Ni-N3-Ni results in ferromagnetic behavior.
2009-08-03
4-Acetyl-pyridinium perchlorate.
2009-07-08
4-Acetyl-pyridine-fumaric acid (2/1).
2009-06-06
Novel trans-dichloridoplatinum(II) complexes with 3- and 4-acetylpyridine: Synthesis, characterization, DFT calculations and cytotoxicity.
2009-05
3-Fluoro-benzoic acid-4-acetyl-pyridine (1/1) at 100 K.
2009-01-23
Hydrogen-bonded assemblies of 20-(4-pyridyl)porphyrin-5(4),10(4),15(4)-tribenzoic acid with dimethyl sulfoxide and 4-acetylpyridine in their dimethyl sulfoxide and tetrahydrofuran solvates.
2007-07
Water induces a structural conversion and accelerates the oxygenation of carboxylate-bridged non-heme diiron enzyme synthetic analogues.
2006-08-07
Synthesis, anti-inflammatory and analgesic activity evaluation of some amidine and hydrazone derivatives.
2006-07-01
Cyanoacetic acid hydrazones of 3-(and 4-)acetylpyridine and some derived ring systems as potential antitumor and anti-HCV agents.
2006-01
Novel milrinone analogs of pyridine-3-carbonitrile derivatives as promising cardiotonic agents.
2005-12
Purification and characterization of rat liver enzyme catalyzing stereoselective reduction of acetylpyridines.
2005-10
Mono- and dinuclear tricarbonyltechnetium(I) complexes with thiosemicarbazones.
2005-02-21
Synthesis and anticonvulsant evaluation of some new 2-substituted-3-arylpyrido[2,3-d]pyrimidinones.
2004-11-01
Syntheses of 2-substituted indoles and fused indoles by photostimulated reactions of o-iodoanilines with carbanions by the SRN1 mechanism.
2003-04-04
Spectral studies of semicarbazones derived from 3- and 4-formylpyridine and 3- and 4-acetylpyridine: crystal and molecular structure of 3-formylpyridine semicarbazone.
2001-08
Construction of Ru(II) Polypyridyl Based Macrocycles: Synthesis, Characterization, Electrochemical, Li Binding, Antitumour and Anti-HIV properties.
2001
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:48:23 GMT 2025
Edited
by admin
on Mon Mar 31 18:48:23 GMT 2025
Record UNII
G47437IOW7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-ACETYLPYRIDINE
Systematic Name English
NSC-111
Preferred Name English
4-PYRIDYL METHYL KETONE
Systematic Name English
KETONE, METHYL 4-PYRIDYL
Systematic Name English
1-(4-PYRIDINYL)ETHANONE
Systematic Name English
ETHANONE, 1-(4-PYRIDINYL)-
Systematic Name English
ACETYL PYRIDINE, 4-
Common Name English
METHYL 4-PYRIDYL KETONE
Systematic Name English
Code System Code Type Description
NSC
111
Created by admin on Mon Mar 31 18:48:23 GMT 2025 , Edited by admin on Mon Mar 31 18:48:23 GMT 2025
PRIMARY
ECHA (EC/EINECS)
214-350-9
Created by admin on Mon Mar 31 18:48:23 GMT 2025 , Edited by admin on Mon Mar 31 18:48:23 GMT 2025
PRIMARY
FDA UNII
G47437IOW7
Created by admin on Mon Mar 31 18:48:23 GMT 2025 , Edited by admin on Mon Mar 31 18:48:23 GMT 2025
PRIMARY
CAS
1122-54-9
Created by admin on Mon Mar 31 18:48:23 GMT 2025 , Edited by admin on Mon Mar 31 18:48:23 GMT 2025
PRIMARY
PUBCHEM
14282
Created by admin on Mon Mar 31 18:48:23 GMT 2025 , Edited by admin on Mon Mar 31 18:48:23 GMT 2025
PRIMARY
EPA CompTox
DTXSID0022147
Created by admin on Mon Mar 31 18:48:23 GMT 2025 , Edited by admin on Mon Mar 31 18:48:23 GMT 2025
PRIMARY