Diethyl 3-(Benzyloxy)cyclobutane-1,1-dicarboxylate CAS 54166-15-3

Purity 97%+In StockPharmaceutical Standards
CAS No.54166-15-3
Molecular FormulaC17H22O5
Molecular Weight306.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Diethyl 3-(Benzyloxy)cyclobutane-1,1-dicarboxylate CAS 54166-15-3 chemical structure

Description

The molecular framework of Diethyl 3-(Benzyloxy)cyclobutane-1,1-dicarboxylate (C17H22O5) is characterized by a flavonoid core, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies Diethyl 3-(Benzyloxy)cyclobutane-1,1-dicarboxylate (CAS 54166-15-3), a certified reference material (molecular formula C17H22O5, MW 306.35 g/mol) for analytical method development and quality control.

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 Diethyl 3-(Benzyloxy)cyclobutane-1,1-dicarboxylate 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 FormulaC17H22O5
Molecular Weight306.35 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
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1972

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