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:
Molecular Weight:
155.20
Beilstein:
110490
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
crystals
bp
274-275 °C (lit.)
mp
69-73 °C (lit.)
SMILES string
c1ccc(cc1)-c2ccncc2
InChI
1S/C11H9N/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h1-9H
InChI key
JVZRCNQLWOELDU-UHFFFAOYSA-N
Gene Information
human ... MMP3(4314)
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Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Daniel Ejarque et al.
Molecules (Basel, Switzerland), 25(16) (2020-08-14)
The synthesis and characterization of one coordination polymer and two trinuclear complexes are presented. The coordination polymer [Zn2(µ-O,O'-ACA)2(ACA)2(4-Phpy)2]n (1) has been obtained by the reaction between Zn(OAc)2·2H2O, α-acetamidocinnamic acid (HACA), and 4-phenylpyridine (4-Phpy) using EtOH as solvent. Its recrystallization in
Dengmeng Song et al.
ChemSusChem, 13(2), 394-399 (2019-11-05)
The fabrication of efficient and convenient photocatalytic H2 evolution systems is a fascinating research topic in the field of solar energy conversion. A ternary self-assembled photocatalytic H2 evolution system was fabricated through supramolecular host-guest chemistry. The system consisted of the
R R Ramsay et al.
Biochemical and biophysical research communications, 146(1), 53-60 (1987-07-15)
The neurotoxicity of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, an impurity in an illicit drug, is expressed after its oxidation to 1-methyl-4-phenylpyridinium by monoamine oxidase. The pyridinium is concentrated by carrier-mediated transport into the mitochondria where it inhibits NADH dehydrogenase and, hence, ATP synthesis. Some
I Irwin et al.
Life sciences, 40(8), 731-740 (1987-02-23)
Because of the chemical and structural similarity between 4-phenylpyridine (4PP) and 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), the effects of 4PP alone and in combination with MPTP on striatal dopamine (DA) concentrations were studied in mice. 4PP did not deplete striatal DA, even when
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
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