131652
Pyridine N-oxide
95%
Sinónimos:
Pyridine oxide
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About This Item
Fórmula empírica (notación de Hill):
C5H5NO
Número de CAS:
Peso molecular:
95.10
Beilstein:
105257
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:
NACRES:
NA.22
Productos recomendados
Nivel de calidad
Ensayo
95%
Formulario
solid
bp
270 °C (lit.)
mp
62-67 °C (lit.)
cadena SMILES
[O-][n+]1ccccc1
InChI
1S/C5H5NO/c7-6-4-2-1-3-5-6/h1-5H
Clave InChI
ILVXOBCQQYKLDS-UHFFFAOYSA-N
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Descripción general
Pyridine N-oxide axle with [2]rotaxanes was synthesized via an anion templated threading-followed-by-stoppering strategy.
Aplicación
Pyridine N-oxide was used to study the FTIR spectra of pyridine N-oxide in acetonitrile.
Código de clase de almacenamiento
11 - Combustible Solids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
289.4 °F - closed cup
Punto de inflamabilidad (°C)
143 °C - closed cup
Equipo de protección personal
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)
Allyn T Londregan et al.
Organic letters, 13(7), 1840-1843 (2011-03-08)
A general and facile one-pot procedure for the synthesis of 2-substituted pyridines from the corresponding pyridine-N-oxides and nucleophiles is presented as a mild alternative to S(N)Ar chemistry. A variety of nucleophiles and heterocyclic-N-oxides participate effectively in this transformation, which uses
Wei Liu et al.
Organic letters, 15(18), 4682-4685 (2013-09-12)
A highly efficient protocol for C-H/C-H cross-coupling has been found to occur between 2-aryl-1,2,3-triazole N-oxides and pyridine N-oxide derivatives. In addition, two homocoupling reactions of 2-substituted 1,2,3-triazole N-oxides and some pyridine N-oxide derivatives were developed. A possible pathway of C-H/C-H
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