CAS 136422-65-6
:3-(4-methoxybenzyl)piperidine
Description:
3-(4-Methoxybenzyl)piperidine is an organic compound characterized by its piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle. The presence of a 4-methoxybenzyl group at the third position of the piperidine ring contributes to its unique properties. This compound typically exhibits a moderate polarity due to the methoxy group, which can influence its solubility in various solvents. It may also display interesting biological activities, making it a subject of interest in medicinal chemistry. The methoxy group can enhance lipophilicity, potentially affecting the compound's pharmacokinetics and interactions with biological targets. Additionally, the structure suggests that it may participate in hydrogen bonding due to the nitrogen atom in the piperidine ring, which can further influence its reactivity and interactions in chemical processes. Overall, 3-(4-methoxybenzyl)piperidine is a versatile compound with potential applications in drug development and synthesis.
Formula:C13H19NO
InChI:InChI=1/C13H19NO/c1-15-13-6-4-11(5-7-13)9-12-3-2-8-14-10-12/h4-7,12,14H,2-3,8-10H2,1H3
SMILES:COc1ccc(cc1)CC1CCCNC1
Synonyms:- Piperidine, 3-[(4-Methoxyphenyl)Methyl]-
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Found 4 products.
3-(4-Methoxy-benzyl)-piperidine
CAS:<p>3-(4-Methoxy-benzyl)-piperidine</p>Purity:≥95%Molecular weight:205.30g/mol3-(4-Methoxybenzyl)piperidine
CAS:<p>3-(4-Methoxybenzyl)piperidine is an active compound that has been shown to have a number of different profiles. It is a synthetic molecule that has been shown to be effective in the treatment of asthma, inflammation, and cancer. 3-(4-Methoxybenzyl)piperidine also has a number of modifications that provide it with different biological functions, including analgesic and anti-inflammatory effects. The structure activity relationship (SAR) for 3-(4-methoxybenzyl)piperidine is strong and it interacts with the active site of the enzyme.</p>Formula:C13H19NOPurity:Min. 95%Molecular weight:205.3 g/mol



