CAS 31252-42-3
:4-Benzylpiperidine
Description:
4-Benzylpiperidine is an organic compound characterized by its piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle, substituted with a benzyl group at the 4-position. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It has a molecular formula that reflects its structure, containing both carbon and nitrogen atoms. 4-Benzylpiperidine is known for its potential applications in medicinal chemistry, particularly in the development of psychoactive substances and as a precursor in the synthesis of various pharmaceuticals. The compound exhibits basic properties due to the presence of the nitrogen atom in the piperidine ring, allowing it to form salts with acids. Its solubility characteristics can vary, but it is generally soluble in organic solvents. Safety data indicates that, like many piperidine derivatives, it should be handled with care due to potential toxicity and the need for proper laboratory safety protocols.
Formula:C12H17N
InChI:InChI=1S/C12H17N/c1-2-4-11(5-3-1)10-12-6-8-13-9-7-12/h1-5,12-13H,6-10H2
InChI key:InChIKey=ABGXADJDTPFFSZ-UHFFFAOYSA-N
SMILES:C(C1=CC=CC=C1)C2CCNCC2
Synonyms:- 4-(Phenylmethyl)piperidine
- 4-Benzyl piperidine
- 4-Benzylpiperidinium
- NSC 30346
- Piperidine, 4-(phenylmethyl)-
- Piperidine, 4-benzyl-
- 4-Benzylpiperidine
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Found 5 products.
4-Benzylpiperidine
CAS:Controlled Product<p>4-Benzylpiperidine is a chemical compound belonging to the class of monoamine neurotransmitters. It has been shown to have antinociceptive properties in vitro and in vivo, as well as potent inhibition of dopamine uptake with an IC50 value of 0.1 μM. 4-Benzylpiperidine has been shown to inhibit inflammation by autophagy induction and activation of antiinflammatory pathways. This compound has also been shown to display potent inhibition activity against 4-hydroxycinnamic acid, which is implicated in the prevention and treatment of inflammatory diseases. 4-Benzylpiperidine exhibits reversible inhibition against monoamine oxidase (MAO) A and MAO B, with IC50 values of 0.02 mM and 2 mM respectively.</p>Formula:C12H17NPurity:Min. 98%Color and Shape:Clear LiquidMolecular weight:175.27 g/mol




