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Details

Stereochemistry ACHIRAL
Molecular Formula C5H5NO
Molecular Weight 95.0993
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PYRIDINE N-OXIDE

SMILES

[O-][N+]1=CC=CC=C1

InChI

InChIKey=ILVXOBCQQYKLDS-UHFFFAOYSA-N
InChI=1S/C5H5NO/c7-6-4-2-1-3-5-6/h1-5H

HIDE SMILES / InChI

Molecular Formula C5H5NO
Molecular Weight 95.0993
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Modulation of the luminescence quantum efficiency for blue luminophor {Al(salophen)}(+) by ester-substituents.
2010-02-28
Densely packed Gd(III)-chelates with fast water exchange on a calix[4]arene scaffold: a potential MRI contrast agent.
2010-01-07
Discovery of 3-methyl-N-(1-oxy-3',4',5',6'-tetrahydro-2'H-[2,4'-bipyridine]-1'-ylmethyl)benzamide (ABT-670), an orally bioavailable dopamine D4 agonist for the treatment of erectile dysfunction.
2006-12-14
Synthesis development of a naphthyridinone p38 kinase inhibitor.
2006-11
Calculations on the group 15 intraring substituted benzenes (pyridine to bismin series) and their datively bonded oxides and sulfides.
2005-10-13
In vitro microsomal metabolic studies on a selective mGluR5 antagonist MTEP: characterization of in vitro metabolites and identification of a novel thiazole ring opening aldehyde metabolite.
2005-08
Enantioselective approach to the hetisine alkaloids. Synthesis of the 3-methyl-1-aza-tricyclo[5.2.1.0(3,8)]decane core via intramolecular dipolar cycloaddition.
2005-07-21
Evidence of the electronic factor for the highly enantioselective catalytic efficiency of Cinchona-derived phase-transfer catalysts.
2005-03-17
1H NMR and DFT study of proton exchange in heterogeneous structures of pyridine-N-oxide/HCl/DCl/H2O.
2005-03
Metal-organic rotaxane frameworks: three-dimensional polyrotaxanes from lanthanide-ion nodes, pyridinium N-oxide axles, and crown-ether wheels.
2005-01-28
HIV-chemotherapy and -prophylaxis: new drugs, leads and approaches.
2004-09
CYP1A1 induction by pyridine and its metabolites in HepG2 cells.
2002-08-15
Evidence for elevation of cytochrome P4502E1 (alcohol-inducible form) mRNA levels in rat kidney following pyridine administration.
1992-07-31
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:44:40 GMT 2025
Edited
by admin
on Mon Mar 31 18:44:40 GMT 2025
Record UNII
91F12JJJ4H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PYRIDINE 1-OXIDE
MI  
Preferred Name English
PYRIDINE N-OXIDE
Systematic Name English
NSC-18250
Code English
PYRIDINE 1-OXIDE [MI]
Common Name English
Code System Code Type Description
WIKIPEDIA
Pyridine-N-oxide
Created by admin on Mon Mar 31 18:44:40 GMT 2025 , Edited by admin on Mon Mar 31 18:44:40 GMT 2025
PRIMARY
NSC
18250
Created by admin on Mon Mar 31 18:44:40 GMT 2025 , Edited by admin on Mon Mar 31 18:44:40 GMT 2025
PRIMARY
CHEBI
29136
Created by admin on Mon Mar 31 18:44:40 GMT 2025 , Edited by admin on Mon Mar 31 18:44:40 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-774-6
Created by admin on Mon Mar 31 18:44:40 GMT 2025 , Edited by admin on Mon Mar 31 18:44:40 GMT 2025
PRIMARY
CAS
694-59-7
Created by admin on Mon Mar 31 18:44:40 GMT 2025 , Edited by admin on Mon Mar 31 18:44:40 GMT 2025
PRIMARY
PUBCHEM
12753
Created by admin on Mon Mar 31 18:44:40 GMT 2025 , Edited by admin on Mon Mar 31 18:44:40 GMT 2025
PRIMARY
FDA UNII
91F12JJJ4H
Created by admin on Mon Mar 31 18:44:40 GMT 2025 , Edited by admin on Mon Mar 31 18:44:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID3061007
Created by admin on Mon Mar 31 18:44:40 GMT 2025 , Edited by admin on Mon Mar 31 18:44:40 GMT 2025
PRIMARY
MESH
C013229
Created by admin on Mon Mar 31 18:44:40 GMT 2025 , Edited by admin on Mon Mar 31 18:44:40 GMT 2025
PRIMARY
MERCK INDEX
m9354
Created by admin on Mon Mar 31 18:44:40 GMT 2025 , Edited by admin on Mon Mar 31 18:44:40 GMT 2025
PRIMARY Merck Index