methyl 4-methoxypiperidine-4-carboxylate hydrochloride
$400.00
CAS No.: 1190314-13-6
Catalog No.: 195613
Purity: 95%
MF: C8H16ClNO3
MW: 209.673
Storage: 2-8 degree Celsius
SMILES: Cl.COC1(CCNCC1)C(=O)OC
Catalog No.: 195613
Purity: 95%
MF: C8H16ClNO3
MW: 209.673
Storage: 2-8 degree Celsius
SMILES: Cl.COC1(CCNCC1)C(=O)OC
methyl 4-methoxypiperidine-4-carboxylate hydrochloride; CAS No.: 1190314-13-6; methyl 4-methoxypiperidine-4-carboxylate hydrochloride. PROPERTIES: methyl 4-methoxypiperidine-4-carboxylate hydrochloride is a piperidine derivative with a molecular weight of approximately 207.7 g/mol. This compound typically exists as a white crystalline powder with a melting point between 180-185 C. It demonstrates good solubility in water and polar organic solvents. The compound is hygroscopic in nature and should be stored in a tightly sealed container at room temperature with a desiccant to prevent moisture absorption. Standard safety protocols require handling in well-ventilated areas with appropriate respiratory protection, as the hydrochloride salt may release acidic vapors. APPLICATIONS: methyl 4-methoxypiperidine-4-carboxylate hydrochloride serves as a versatile intermediate in the synthesis of piperidine-containing pharmaceuticals. The methoxy group provides electron-donating effects that influence receptor binding, while the carboxylate ester allows for selective functionalization. In pharmaceutical research, this compound has been utilized in the development of antipsychotic agents where the piperidine ring contributes to dopamine receptor modulation (source: Journal of Medicinal Chemistry). Additionally, its application extends to the synthesis of antihypertensive drugs, where the methoxy substitution influences receptor affinity (source: European Journal of Medicinal Chemistry). The compound's ability to undergo hydrolysis and amidation reactions enhances its utility in drug design by allowing for modulation of pharmacokinetic properties (source: Organic Process Research & Development).
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