131652
Pyridine N-oxide
95%
Synonym(s):
Pyridine oxide
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About This Item
Empirical Formula (Hill Notation):
C5H5NO
CAS Number:
Molecular Weight:
95.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-774-6
Beilstein/REAXYS Number:
105257
MDL number:
Assay:
95%
Form:
solid
InChI key
ILVXOBCQQYKLDS-UHFFFAOYSA-N
InChI
1S/C5H5NO/c7-6-4-2-1-3-5-6/h1-5H
SMILES string
[O-][n+]1ccccc1
assay
95%
form
solid
bp
270 °C (lit.)
Quality Level
Related Categories
General description
Pyridine N-oxide axle with [2]rotaxanes was synthesized via an anion templated threading-followed-by-stoppering strategy.
Application
Pyridine N-oxide was used to study the FTIR spectra of pyridine N-oxide in acetonitrile.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
289.4 °F - closed cup
flash_point_c
143 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Jan Balzarini et al.
The Journal of antimicrobial chemotherapy, 55(2), 135-138 (2005-01-15)
Pyridine N-oxide derivatives represent a new class of anti-HIV compounds, for which some members exclusively act through inhibition of HIV-1 reverse transcriptase and thus characteristically behave as non-nucleoside reverse transcriptase inhibitors. Other members act, additionally or alternatively, at a post-integrational
G Pitsevich et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 120, 585-594 (2014-01-01)
FTIR spectra of pyridine N-oxide and trichloroacetic acid H-bonded complex in acetonitrile were studied at 20 and 50°C. The calculations of equilibrium configurations of the complex and their IR spectra in harmonic- and anharmonic approximations were carried out at the
Highly efficient gold nanoparticle catalyzed deoxygenation of amides, sulfoxides, and pyridine N-oxides.
Yusuke Mikami et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(6), 1768-1772 (2011-01-29)
Masahito Murai et al.
Chemical communications (Cambridge, England), 48(61), 7622-7624 (2012-06-26)
Gold(I)-catalysed tandem oxygen-transfer/cycloisomerisation reaction of 2-(2-propynyl)pyridine N-oxides provides an atom-economical route to indolizinone frameworks.
Palladium-catalyzed (N-oxido-2-pyridinyl)methyl transfer from 2-(2-hydroxyalkyl)pyridine N-oxide to aryl halides by beta-carbon elimination.
Takafumi Suehiro et al.
Chemistry, an Asian journal, 4(8), 1217-1220 (2009-06-09)
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