3-(4-Nitro-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester CAS 405887-36-7

Purity 97%+In StockPharmaceutical Standards
CAS No.405887-36-7
Molecular FormulaC15H20N2O5
Molecular Weight308.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Nitro-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester CAS 405887-36-7 chemical structure

Description

3-(4-Nitro-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester (CAS 405887-36-7) is a high-purity analytical reference standard with the molecular formula C15H20N2O5 and a molecular weight of 308.33 g/mol.

Structurally, 3-(4-Nitro-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester (C15H20N2O5) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 308.33 g/mol, it falls into the moderately-high-molecular-weight range. 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).

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.

As a certified reference material (CRM), 3-(4-Nitro-phenoxy)-pyrrolidine-1-carboxylic acid tert-butyl ester meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC15H20N2O5
Molecular Weight308.33 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms2

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