tert-Butyl 3-oxo-2-(2-oxo-2-(2-phenoxyethoxy)ethyl)piperazine-1-carboxylate CAS 1009751-17-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1009751-17-0
Molecular FormulaC19H26N2O6
Molecular Weight378.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 3-oxo-2-(2-oxo-2-(2-phenoxyethoxy)ethyl)piperazine-1-carboxylate CAS 1009751-17-0 chemical structure

Description

CATO manufactures tert-Butyl 3-oxo-2-(2-oxo-2-(2-phenoxyethoxy)ethyl)piperazine-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.

tert-Butyl 3-oxo-2-(2-oxo-2-(2-phenoxyethoxy)ethyl)piperazine-1-carboxylate (CAS 1009751-17-0), molecular formula C19H26N2O6 and molecular weight 378.42 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a flavonoid core, an amide group, a hydroxyl group, an ether linkage, tert-Butyl 3-oxo-2-(2-oxo-2-(2-phenoxyethoxy)ethyl)piperazine-1-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 378.42 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC19H26N2O6
Molecular Weight378.42 g/mol
AppearancePale yellow to 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms2

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