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131652

吡啶 N-氧化物

95%

别名:

Pyridine oxide

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关于此项目

经验公式（希尔记法）:
C5H5NO
化学文摘社编号:
694-59-7
分子量:
95.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24848028
EC Number:
211-774-6
Beilstein/REAXYS Number:
105257
MDL number:
MFCD00006194
Assay:
95%
Form:
solid
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Quality Level

100

assay

95%

form

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

General description

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。

Application

吡啶N-氧化物用于研究吡啶N-氧化物在乙腈中的FTIR光谱。

存储类别

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
WXBF8772V
WXBF7568V
WXBF5351V
WXBF4147V
WXBF0278V

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Jinshui Chen et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(30), 7268-7276 (2009-07-07)
Optically active chiral alkyl chlorides are valuable compounds because of their bioactivity and versatile synthetic utility. Accordingly, the ring opening of epoxides with a chloride nucleophile stands as an important goal in asymmetric catalysis. We describe herein recent advances in
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.
Xue Gong et al.
Organic letters, 13(7), 1766-1769 (2011-03-11)
A Pd(II)-catalyzed oxidative coupling between pyridine N-oxides and N-substituted indoles via 2-fold C-H bond activation was achieved with high selectivity using Ag(2)CO(3) as an oxidant.
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全球贸易项目编号

货号GTIN
131652-100G04061838728487
131652-25G04061838728494