CAS 4350-41-8
:2-[(4-Chlorophenyl)methyl]pyridine
Description:
2-[(4-Chlorophenyl)methyl]pyridine, also known by its CAS number 4350-41-8, is an organic compound characterized by a pyridine ring substituted with a 4-chlorobenzyl group. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as ethanol and dichloromethane, but has limited solubility in water due to its hydrophobic nature. The presence of the chlorophenyl group enhances its lipophilicity, which can influence its biological activity and interactions. It is often studied for its potential applications in pharmaceuticals and agrochemicals, as the structural features may impart specific biological properties. The compound may also exhibit moderate to high stability under standard conditions, although it should be handled with care due to the presence of chlorine, which can pose environmental and health risks. Overall, 2-[(4-Chlorophenyl)methyl]pyridine serves as an interesting subject for research in medicinal chemistry and related fields.
Formula:C12H10ClN
InChI:InChI=1/C12H10ClN/c13-11-6-4-10(5-7-11)9-12-3-1-2-8-14-12/h1-8H,9H2
InChI key:InChIKey=XSVWMIMFDMJQRL-UHFFFAOYSA-N
SMILES:C(C1=CC=C(Cl)C=C1)C2=CC=CC=N2
Synonyms:- 2-[(4-Chlorophenyl)methyl]pyridine
- 2-(4-Chlorobenzyl)pyridine
- 2-(p-Chlorobenzyl)pyridine
- Pyridine, 2-[(4-chlorophenyl)methyl]-
- Pyridine, 2-(p-chlorobenzyl)-
- 4-CHLOROPHENYL 4-PYRIDYL KETONE
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Found 5 products.
2-(4-Chlorobenzyl)pyridine
CAS:Formula:C12H10ClNPurity:98%Color and Shape:LiquidMolecular weight:203.66752-(4-Chlorobenzyl)pyridine
CAS:Controlled Product<p>Applications 2-(4-CHLOROBENZYL)PYRIDINE (cas# 4350-41-8) is a useful research chemical.<br></p>Formula:C12H10NClColor and Shape:NeatMolecular weight:203.662-(4-Chlorobenzyl)pyridine
CAS:<p>2-(4-Chlorobenzyl)pyridine is a synthetic pyridine compound that has been shown to have anti-cancer properties. It is also a potent inducer of the enzyme methane monooxygenase and has been shown to interact with other compounds, such as maleates and sulfoxides, which are also used in this type of experiment. The catalytic mechanism for 2-(4-chlorobenzyl)pyridine is not yet known, but it may involve an acidic chlorine atom or a hydrochloric acid catalyst. 2-(4-Chlorobenzyl)pyridine has been found to be effective at inhibiting the growth of cancer cells in vitro without toxic effects on healthy cells. It has also been shown to inhibit the proliferation of human leukemia cells in vivo.</p>Formula:C12H10ClNPurity:Min. 95%Molecular weight:203.67 g/mol




