tert-Butyl 4-(2-methoxy-2-oxoethyl)-3-oxopiperidine-1-carboxylate CAS 1159983-58-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1159983-58-0
Molecular FormulaC13H21NO5
Molecular Weight271.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 4-(2-methoxy-2-oxoethyl)-3-oxopiperidine-1-carboxylate CAS 1159983-58-0 chemical structure

Description

The molecular framework of tert-Butyl 4-(2-methoxy-2-oxoethyl)-3-oxopiperidine-1-carboxylate (C13H21NO5) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

tert-Butyl 4-(2-methoxy-2-oxoethyl)-3-oxopiperidine-1-carboxylate (CAS 1159983-58-0) is a high-purity analytical reference standard with the molecular formula C13H21NO5 and a molecular weight of 271.31 g/mol.

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

CATO manufactures tert-Butyl 4-(2-methoxy-2-oxoethyl)-3-oxopiperidine-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.

Physical & Chemical Properties

Molecular FormulaC13H21NO5
Molecular Weight271.31 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 methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms1

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