209732
3-Phenylpyridine
97%
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About This Item
Empirical Formula (Hill Notation):
C11H9N
CAS Number:
Molecular Weight:
155.20
EC Number:
213-762-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
110400
MDL number:
Assay:
97%
Form:
liquid
InChI key
HJKGBRPNSJADMB-UHFFFAOYSA-N
InChI
1S/C11H9N/c1-2-5-10(6-3-1)11-7-4-8-12-9-11/h1-9H
SMILES string
c1ccc(cc1)-c2cccnc2
assay
97%
form
liquid
refractive index
n20/D 1.616 (lit.)
bp
269-270 °C/749 mmHg (lit.)
density
1.082 g/mL at 25 °C (lit.)
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General description
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.
Application
3-Phenylpyridine was employed as axial ligand to investigate the rate of olefin oxygenation catalyzed by synthetic metalloporphyrins.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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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
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
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
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