(3S,4S)-tert-butyl 3-(benzyl(benzyloxycarbonyl)amino)-4-hydroxypyrrolidine-1-carboxylate CAS 708273-38-5

Purity 97%+In StockPharmaceutical Standards
CAS No.708273-38-5
Molecular FormulaC24H30N2O5
Molecular Weight426.51 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3S,4S)-tert-butyl 3-(benzyl(benzyloxycarbonyl)amino)-4-hydroxypyrrolidine-1-carboxylate CAS 708273-38-5 chemical structure

Description

CATO supplies (3S,4S)-tert-butyl 3-(benzyl(benzyloxycarbonyl)amino)-4-hydroxypyrrolidine-1-carboxylate (CAS 708273-38-5), a certified reference material (molecular formula C24H30N2O5, MW 426.51 g/mol) for analytical method development and quality control.

Owing to a flavonoid core, an amide group, a hydroxyl group, an ether linkage, (3S,4S)-tert-butyl 3-(benzyl(benzyloxycarbonyl)amino)-4-hydroxypyrrolidine-1-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 426.51 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC24H30N2O5
Molecular Weight426.51 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Nitrogen Atoms2

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