2-Phenyl-3-styryl-5-(p-tolyl)isoxazolidine CAS 120781-95-5

Purity 97%+In StockPharmaceutical Standards
CAS No.120781-95-5
Molecular FormulaC24H23NO
Molecular Weight341.45 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Phenyl-3-styryl-5-(p-tolyl)isoxazolidine CAS 120781-95-5 chemical structure

Description

The occurrence of 2-Phenyl-3-styryl-5-(p-tolyl)isoxazolidine is closely related to a steroid core, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

2-Phenyl-3-styryl-5-(p-tolyl)isoxazolidine (CAS 120781-95-5) is a high-purity analytical reference standard with the molecular formula C24H23NO and a molecular weight of 341.45 g/mol.

The molecular framework of 2-Phenyl-3-styryl-5-(p-tolyl)isoxazolidine (C24H23NO) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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).

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.

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 FormulaC24H23NO
Molecular Weight341.45 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms1

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