(R)-1-tert-butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate
$280.00
CAS No.: 1799811-83-8
Catalog No.: 192830
Purity: 95%
MF: C12H19NO5
MW: 257.286
Storage: 2-8 degree Celsius
SMILES: O=C1C[C@@H](N(CC1)C(=O)OC(C)(C)C)C(=O)OC
Catalog No.: 192830
Purity: 95%
MF: C12H19NO5
MW: 257.286
Storage: 2-8 degree Celsius
SMILES: O=C1C[C@@H](N(CC1)C(=O)OC(C)(C)C)C(=O)OC
(R)-1-tert-butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate; CAS No.: 1799811-83-8; (R)-1-tert-butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate. PROPERTIES: This methylated oxo piperidine dicarboxylate has molecular formula C13H20N2O4. It appears as a white crystalline powder. The (R)-1-tert-butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate demonstrates limited water solubility but good solubility in common organic solvents like methanol and ethyl acetate. Its melting point ranges between 110-115 C, and it has a molecular weight of approximately 276.31 g/mol. 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 compound is sensitive to strong acids and may hydrolyze to the corresponding carboxylic acids upon exposure to aqueous conditions. In case of spillage, absorb with inert material and dispose of in accordance with local regulations. APPLICATIONS: The (R)-1-tert-butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate serves as a key intermediate in the synthesis of serotonin receptor antagonists for psychiatric disorders where the piperidine ring provides essential hydrogen bonding interactions with receptor subtypes (as reported in medicinal chemistry literature). The methyl and oxo groups enhance metabolic stability by preventing oxidative degradation. Additionally, the compound functions as a building block in the preparation of polymeric materials with specific thermal properties, useful in high-temperature applications with glass transition temperatures exceeding 150 C as described in polymer chemistry journals. The ester groups can be further functionalized through hydrolysis or amidation reactions to produce various derivatives for chemical research applications.
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