(2R,3R)-tert-Butyl 3-amino-2-phenylpiperidine-1-carboxylate CAS 1621232-39-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1621232-39-0
Molecular FormulaC16H24N2O2
Molecular Weight276.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2R,3R)-tert-Butyl 3-amino-2-phenylpiperidine-1-carboxylate CAS 1621232-39-0 chemical structure

Description

CATO manufactures (2R,3R)-tert-Butyl 3-amino-2-phenylpiperidine-1-carboxylate under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

(2R,3R)-tert-Butyl 3-amino-2-phenylpiperidine-1-carboxylate (CAS 1621232-39-0) is a high-purity analytical reference standard with the molecular formula C16H24N2O2 and a molecular weight of 276.37 g/mol.

(2R,3R)-tert-Butyl 3-amino-2-phenylpiperidine-1-carboxylate (C16H24N2O2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC16H24N2O2
Molecular Weight276.37 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Nitrogen Atoms2

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