CAS 50585-91-6

methyl 1-benzylpiperidine-3-carboxylate

Description:

Methyl 1-benzylpiperidine-3-carboxylate, identified by its CAS number 50585-91-6, is a chemical compound that belongs to the class of piperidine derivatives. It features a piperidine ring, which is a six-membered nitrogen-containing heterocycle, substituted with a benzyl group and a carboxylate moiety. This compound is typically characterized by its moderate polarity due to the presence of both hydrophobic (benzyl) and hydrophilic (carboxylate) groups. It may exhibit solubility in organic solvents such as ethanol and dichloromethane, while being less soluble in water. Methyl 1-benzylpiperidine-3-carboxylate may also display biological activity, making it of interest in medicinal chemistry and pharmacology. Its structural features suggest potential interactions with biological targets, which could be explored for therapeutic applications. As with many organic compounds, safety and handling precautions should be observed, as the specific toxicity and environmental impact of this compound may not be fully characterized.

Formula: C₁₄H₁₉NO₂

InChI: InChI=1/C14H19NO2/c1-17-14(16)13-8-5-9-15(11-13)10-12-6-3-2-4-7-12/h2-4,6-7,13H,5,8-11H2,1H3

SMILES: COC(=O)C1CCCN(Cc2ccccc2)C1

Synonyms:

• 3-Piperidinecarboxylic acid, 1-(phenylmethyl)-, methyl ester
• Methyl 1-benzylpiperidine-3-carboxylate

3-​Piperidinecarboxylic acid, 1-​(phenylmethyl)​-​, methyl ester

CAS: 50585-91-6

Formula: C₁₄H₁₉NO₂

Purity: 97%

Color and Shape: Liquid

Molecular weight: 233.3062

Ref: IN-DA006XV0

Methyl 1-Benzyl-Piperidine-3-Carboxylate

CAS: 50585-91-6

Methyl 1-Benzyl-Piperidine-3-Carboxylate

Purity: 97%

Molecular weight: 233.31g/mol

Ref: 54-OR1013768

Methyl 1-benzylpiperidine-3-carboxylate

CAS: 50585-91-6

Formula: C₁₄H₁₉NO₂

Purity: 97%+(GC-MS);RG

Molecular weight: 233.311

Ref: 10-F237177

Methyl 1-benzylpiperidine-3-carboxylate

CAS: 50585-91-6

Methyl 1-benzylpiperidine-3-carboxylate is a neurotoxin that causes Parkinson's disease, which is characterized by the death of dopamine neurons in the substantia nigra. It has been shown to bind to dopamine receptors and inhibit neurotransmission. The biological activity of methyl 1-benzylpiperidine-3-carboxylate was demonstrated as a result of its ability to inhibit the binding of oxadiazole derivatives, which are ligands for these receptors. Methyl 1-benzylpiperidine-3-carboxylate also has an agonistic effect on oxadiazole analogues and increases their biological activity.

Formula: C₁₄H₁₉NO₂

Purity: Min. 95%

Molecular weight: 233.31 g/mol

Ref: 3D-ACA58591