tert-butyl 4-amino-2-isopropylpiperidine-1-carboxylate
$600.00
CAS No.: 1558365-90-4
Catalog No.: 192827
Purity: 95%
MF: C13H26N2O2
MW: 242.363
Storage: 2-8 degree Celsius
SMILES: NC1CC(N(CC1)C(=O)OC(C)(C)C)C(C)C
Catalog No.: 192827
Purity: 95%
MF: C13H26N2O2
MW: 242.363
Storage: 2-8 degree Celsius
SMILES: NC1CC(N(CC1)C(=O)OC(C)(C)C)C(C)C
tert-butyl 4-amino-2-isopropylpiperidine-1-carboxylate; CAS No.: 1558365-90-4; tert-butyl 4-amino-2-isopropylpiperidine-1-carboxylate. PROPERTIES: This amino- and isopropyl-substituted piperidine carbamate has molecular formula C14H26N2O2. It appears as a white crystalline powder. The tert-butyl 4-amino-2-isopropylpiperidine-1-carboxylate demonstrates limited water solubility but good solubility in common organic solvents like methanol and ethyl acetate. Its melting point ranges between 90-95 C, and it has a molecular weight of approximately 258.38 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 undergo carbamate hydrolysis upon exposure to aqueous conditions. In case of spillage, absorb with inert material and dispose of in accordance with local regulations. APPLICATIONS: The tert-butyl 4-amino-2-isopropylpiperidine-1-carboxylate serves as a valuable intermediate in the synthesis of serotonin receptor antagonists for psychiatric disorders where the piperidine ring provides essential hydrogen bonding interactions with receptor subtypes (as detailed in medicinal chemistry literature). The isopropyl group enhances metabolic stability by preventing oxidative degradation. Additionally, the compound functions as a building block in the preparation of chiral ligands for asymmetric catalysis, achieving enantiomeric excesses above 95% in certain hydrogenation reactions as described in synthetic chemistry journals. The carbamate group can be further functionalized through hydrolysis or alkylation reactions to produce various derivatives for chemical research applications.
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