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131652

吡啶 N-氧化物

Name: 吡啶 <I>N</I>-氧化物
Brand: ALDRICH

95%

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别名:

Pyridine oxide

经验公式（希尔记法）:

C₅H₅NO

CAS号:

694-59-7

分子量:

95.10

Beilstein:

105257

EC 号:

211-774-6

MDL编号:

MFCD00006194

PubChem化学物质编号:

24848028

NACRES:

NA.22

检测方案

95%

形式

solid

bp

270 °C (lit.)

mp

62-67 °C (lit.)

SMILES string

[O-][n+]1ccccc1

InChI

1S/C5H5NO/c7-6-4-2-1-3-5-6/h1-5H

InChI key

ILVXOBCQQYKLDS-UHFFFAOYSA-N

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一般描述

具有[2]轮烷的吡啶N-氧化物轴通过阴离子模板化穿线 - 后续 - 加塞策略合成。

应用

吡啶N-氧化物用于研究吡啶N-氧化物在乙腈中的FTIR光谱。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

289.4 °F - closed cup

闪点(°C)

143 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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T1503

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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)

Pyridine N-oxide derivatives: unusual anti-HIV compounds with multiple mechanisms of antiviral action.

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

Pyridine N-oxide/trichloroacetic acid complex in acetonitrile: FTIR spectra, anharmonic calculations and computations of 1-3D potential surfaces of O-H vibrations.

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

Temperature and solvent structure dependence of VO2+ complexes of pyridine-N-oxide derivatives and their interaction with human serum transferrin.

Daniele Sanna et al.

Dalton transactions (Cambridge, England : 2003), 41(24), 7304-7318 (2012-05-12)

The behaviour of the systems formed by VO(2+), 2-hydroxypyridine-N-oxide (Hhpo) and 2-mercaptopyridine-N-oxide (Hmpo) was studied both in solution and in the solid state through the combined application of spectroscopic (EPR and UV-Vis spectroscopy) and DFT methods. The geometry of solid

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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