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209732

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3-Phenylpyridine

97%

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About This Item

Fórmula empírica (Notação de Hill):
C11H9N
Número CAS:
1008-88-4
Peso molecular:
155.20
Beilstein:
110400
Número CE:
213-762-6
Número MDL:
MFCD00006380
Código UNSPSC:
12352100
ID de substância PubChem:
24852590

Ensaio

97%

Formulário

liquid

índice de refração

n20/D 1.616 (lit.)

p.e.

269-270 °C/749 mmHg (lit.)

densidade

1.082 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

c1ccc(cc1)-c2cccnc2

InChI

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

chave InChI

HJKGBRPNSJADMB-UHFFFAOYSA-N

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Descrição geral

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.

Aplicação

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

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

230.0 °F - closed cup

Ponto de fulgor (°C)

110 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
SHBG1409V
SHBB7587V
96898MJ
03320DW
03515DD

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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
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
Surface-enhanced Raman spectroscopy studies of phenylpyridines interacting with a copper electrode surface.
Zawada K and Bukowska J.
Surface Science, 507, 34-39 (2002)
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
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