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Merck
모든 사진(1)

주요 문서

209732

Sigma-Aldrich

3-Phenylpyridine

97%

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About This Item

실험식(Hill 표기법):
C11H9N
CAS Number:
Molecular Weight:
155.20
Beilstein:
110400
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:

분석

97%

양식

liquid

refractive index

n20/D 1.616 (lit.)

bp

269-270 °C/749 mmHg (lit.)

density

1.082 g/mL at 25 °C (lit.)

SMILES string

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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일반 설명

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[1]. Interactions of 3-phenylpyridine with copper surface has been investigated by Surface-enhanced Raman scattering (SERS) spectroscopy and cyclic voltammetry[2]. It is a useful synthetic intermediate.

애플리케이션

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

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

230.0 °F - closed cup

Flash Point (°C)

110 °C - closed cup

개인 보호 장비

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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문서 라이브러리 방문

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
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
Surface-enhanced Raman spectroscopy studies of phenylpyridines interacting with a copper electrode surface.
Zawada K and Bukowska J.
Surface Science, 507, 34-39 (2002)
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
Leszek Pazderski et al.
Magnetic resonance in chemistry : MRC, 47(8), 658-665 (2009-05-28)
1H, 13C and 15N nuclear magnetic resonance studies of gold(III), palladium(II) and platinum(II) chloride complexes with phenylpyridines (PPY: 4-phenylpyridine, 4ppy; 3-phenylpyridine, 3ppy; and 2-phenylpyridine, 2ppy) having the general formulae [Au(PPY)Cl3], trans-/cis-[Pd(PPY)2Cl2] and trans-/cis-[Pt(PPY)2Cl2] were performed and the respective chemical shifts

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