ethyl 2-(2,2-dimethylpiperidin-4-yl)acetate hydrochloride

ethyl 2-(2,2-dimethylpiperidin-4-yl)acetate hydrochloride

tert-butyl 3,3-difluoro-5-oxopiperidine-1-carboxylate

tert-butyl 3,3-difluoro-5-oxopiperidine-1-carboxylate

cis-methyl 6-methylpiperidine-3-carboxylate hydrochloride

$285.00
CAS No.: 1009376-77-5
Catalog No.: 192817
Purity: 95%
MF: C8H16ClNO2
MW: 193.674
Storage: 2-8 degree Celsius
SMILES: Cl.C[C@@H]1CC[C@@H](CN1)C(=O)OC
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cis-methyl 6-methylpiperidine-3-carboxylate hydrochloride; CAS No.: 1009376-77-5; cis-methyl 6-methylpiperidine-3-carboxylate hydrochloride. PROPERTIES: This cis-dimethylated piperidine carboxylate salt has molecular formula C9H16N2O2 {HCl. It appears as a white crystalline powder. The cis-methyl 6-methylpiperidine-3-carboxylate hydrochloride exhibits high water solubility (exceeding 100 mg/mL) and moderate solubility in common polar solvents. Its melting point ranges between 130-135 C (with decomposition), and it has a molecular weight of approximately 204.70 g/mol (free base). When handling, care should be taken to avoid skin contact and use of proper respiratory protection. Storage should be in a tightly sealed container at room temperature, protected from light and moisture. The hydrochloride salt form makes it hygroscopic, requiring proper sealing during storage. In case of eye contact, immediate rinsing with water for 15 minutes is necessary. APPLICATIONS: The cis-methyl 6-methylpiperidine-3-carboxylate hydrochloride functions as a key intermediate in the synthesis of sodium channel blockers for pain management where the piperidine ring provides essential hydrogen bonding interactions with receptor subtypes (as reported in medicinal chemistry literature). The methyl groups enhance metabolic stability by preventing oxidative degradation. Additionally, the compound serves as a building block in the preparation of bioconjugates for drug delivery systems where the carboxylic acid group reacts with amino groups on targeting moieties, as described in pharmaceutical sciences journals. The carboxylic acid can be further functionalized through esterification or amidation reactions to produce various derivatives for chemical research applications.

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