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Merck
CN

P33429

4-Phenylpyridine

97%

Synonym(s):

γ-Phenylpyridine, 1-Benzylhydrazine dihydrochloride, p-Phenylpyridine

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About This Item

Empirical Formula (Hill Notation):
C11H9N
CAS Number:
939-23-1
Molecular Weight:
155.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24898403
EC Number:
213-357-4
Beilstein/REAXYS Number:
110490
MDL number:
MFCD00006420
Assay:
97%
Form:
crystals

Key Documents

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Product Name

4-Phenylpyridine, 97%

InChI

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

InChI key

JVZRCNQLWOELDU-UHFFFAOYSA-N

SMILES string

c1ccc(cc1)-c2ccncc2

assay

97%

form

crystals

bp

274-275 °C (lit.)

mp

69-73 °C (lit.)

Quality Level

100

Gene Information

human ... MMP3(4314)

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ3595
MKCP8457
MKCL8729
MKCD9974
MKCG5135

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Germano Giuliani et al.
Bioorganic & medicinal chemistry, 19(7), 2242-2251 (2011-03-23)
The quinoline nucleus of the previously described 4-phenylquinoline-3-carboxamides NK(1) receptor ligands 7 has been transformed into either substituted or azole-(i.e., triazole or tetrazole) fused pyridine moieties of compounds 9 and 10, respectively, in order to obtain NK(1) receptor ligands showing
K S Hsu et al.
The Journal of pharmacology and experimental therapeutics, 279(2), 740-747 (1996-11-01)
The effect of L-deprenyl (selegiline) on the excitatory synaptic transmission was characterized in the CA1 neurons of rat hippocampal slices by using a intracellular recording technique. Superfusion of L-deprenyl (0.1-10 microM) reversibly decreased the EPSP, which was evoked by orthodromic
A D Vaz et al.
Drug metabolism and disposition: the biological fate of chemicals, 20(1), 108-112 (1992-01-01)
The binding to human placental aromatase cytochrome P-450 and resulting extent of inhibition was examined for pyridine, pyridines substituted at the 2-, 3-, or 4-positions with phenyl or benzoyl groups, and the nonpyridinic structural analogs biphenyl and benzophenone. Spectral binding
Camilla C Golfeto et al.
Journal of inorganic biochemistry, 104(5), 489-495 (2010-02-02)
The synthesis and characterization of ruthenium compounds of the type [RuCl(2)(NO)(dppp)(L)]PF(6) [dppp=1,3-bis(diphenylphosphino)propane; L=pyridine, 4-methylpyridine, 4-phenylpyridine and dimethyl sulfoxide] are described. The complexes were characterized by elemental analysis, UV/Vis and infrared spectroscopy, cyclic voltammetry, and X-ray crystallography for the complexes with
C C Huang et al.
Brain research, 753(1), 27-35 (1997-04-04)
The effects of L-deprenyl (selegiline), a highly selective monoamine oxidase type B (MAO-B) inhibitor, on cell excitability of rat hippocampal CA1 neurons were examined in slice preparations using intracellular recording techniques. Superfusion of L-deprenyl (10 and 20 microM) reversibly limited
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