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Merck
CN

209732

Sigma-Aldrich

3-苯基吡啶

97%

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经验公式(希尔记法):
C11H9N
CAS号:
分子量:
155.20
Beilstein:
110400
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

检测方案

97%

形式

liquid

折射率

n20/D 1.616 (lit.)

bp

269-270 °C/749 mmHg (lit.)

密度

1.082 g/mL at 25 °C (lit.)

SMILES字符串

c1ccc(cc1)-c2cccnc2

InChI

1S/C11H9N/c1-2-5-10(6-3-1)11-7-4-8-12-9-11/h1-9H

InChI key

HJKGBRPNSJADMB-UHFFFAOYSA-N

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一般描述

3-Phenylpyridine forms complexes with gold(III), palladium(II) and platinum(II) chloride and their 1H, 13C and 15N nuclear magnetic resonance studies have been reported. Interactions of 3-phenylpyridine with copper surface has been investigated by Surface-enhanced Raman scattering (SERS) spectroscopy and cyclic voltammetry. It is a useful synthetic intermediate.

应用

3-Phenylpyridine was employed as axial ligand to investigate the rate of olefin oxygenation catalyzed by synthetic metalloporphyrins.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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T L Perry et al.
Journal of the neurological sciences, 85(3), 309-317 (1988-07-01)
Idiopathic Parkinson's disease (PD) is likely to be caused by one or more unidentified neurotoxins, present in the environment or formed endogenously, which progressively damage dopaminergic nigrostriatal neurons. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is an experimental neurotoxin which produces biochemical and neuropathological changes
Marc P Bonaca et al.
Future cardiology, 5(5), 435-442 (2009-09-01)
SCH 530348, a synthetic tricyclic 3-phenylpyridine, is an orally active fourth generation himbacine-based antagonist of the protease-activated receptor (PAR)-1, the primary receptor for thrombin on platelets in humans. SCH 530348 is the first in a new class of compounds that
Sanjeev Kumar et al.
Journal of medicinal chemistry, 51(16), 4968-4977 (2008-07-31)
Indoleamine 2,3-dioxygenase (IDO) is emerging as an important new therapeutic target for the treatment of cancer, chronic viral infections, and other diseases characterized by pathological immune suppression. With the goal of developing more potent IDO inhibitors, a systematic study of
Surface-enhanced Raman spectroscopy studies of phenylpyridines interacting with a copper electrode surface.
Zawada K and Bukowska J.
Surface Science, 507, 34-39 (2002)
J P Collman et al.
Proceedings of the National Academy of Sciences of the United States of America, 80(22), 7039-7041 (1983-11-01)
The rate of olefin oxygenation catalyzed by synthetic metalloporphyrins is examined, employing sodium hypochlorite as the oxygen atom source. The rate of epoxidation and the stability of the catalyst are shown to be dependent on the nature of the axial

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