(R)-3-((9H-fluoren-9-yl)methoxy)-3-oxo-2-((phenylthio)methyl)propanoic acid CAS 488761-06-4

Purity 97%+In StockPharmaceutical Standards
CAS No.488761-06-4
Molecular FormulaC24H20O4S
Molecular Weight404.48 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-3-((9H-fluoren-9-yl)methoxy)-3-oxo-2-((phenylthio)methyl)propanoic acid CAS 488761-06-4 chemical structure

Description

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

CATO supplies (R)-3-((9H-fluoren-9-yl)methoxy)-3-oxo-2-((phenylthio)methyl)propanoic acid (CAS 488761-06-4), a certified reference material (molecular formula C24H20O4S, MW 404.48 g/mol) for analytical method development and quality control.

The molecular framework of (R)-3-((9H-fluoren-9-yl)methoxy)-3-oxo-2-((phenylthio)methyl)propanoic acid (C24H20O4S) is characterized by a flavonoid core, a sulfone 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures (R)-3-((9H-fluoren-9-yl)methoxy)-3-oxo-2-((phenylthio)methyl)propanoic acid 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 FormulaC24H20O4S
Molecular Weight404.48 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
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)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Sulfur Atoms1

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