3-([1,1'-Biphenyl]-4-yl)-2-(3-chlorophenyl)-5-phenylisoxazolidine CAS 629643-19-2

Purity 97%+In StockPharmaceutical Standards
CAS No.629643-19-2
Molecular FormulaC27H22ClNO
Molecular Weight411.92 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-([1,1'-Biphenyl]-4-yl)-2-(3-chlorophenyl)-5-phenylisoxazolidine CAS 629643-19-2 chemical structure

Description

The molecular framework of 3-([1,1'-Biphenyl]-4-yl)-2-(3-chlorophenyl)-5-phenylisoxazolidine (C27H22ClNO) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies 3-([1,1'-Biphenyl]-4-yl)-2-(3-chlorophenyl)-5-phenylisoxazolidine (CAS 629643-19-2), a certified reference material (molecular formula C27H22ClNO, MW 411.92 g/mol) for analytical method development and quality control.

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 FormulaC27H22ClNO
Molecular Weight411.92 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)17.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentCl-containing
Nitrogen Atoms1

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