2-(1-((2-Fluoro-5-(trifluoromethyl)phenyl)imino)ethyl)-3-hydroxy-1H-inden-1-one CAS 1023496-63-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1023496-63-0
Molecular FormulaC18H11F4NO2
Molecular Weight349.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(1-((2-Fluoro-5-(trifluoromethyl)phenyl)imino)ethyl)-3-hydroxy-1H-inden-1-one CAS 1023496-63-0 chemical structure

Description

CATO manufactures 2-(1-((2-Fluoro-5-(trifluoromethyl)phenyl)imino)ethyl)-3-hydroxy-1H-inden-1-one 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.

CATO supplies 2-(1-((2-Fluoro-5-(trifluoromethyl)phenyl)imino)ethyl)-3-hydroxy-1H-inden-1-one (CAS 1023496-63-0), a certified reference material (molecular formula C18H11F4NO2, MW 349.28 g/mol) for analytical method development and quality control.

The molecular framework of 2-(1-((2-Fluoro-5-(trifluoromethyl)phenyl)imino)ethyl)-3-hydroxy-1H-inden-1-one (C18H11F4NO2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

Physical & Chemical Properties

Molecular FormulaC18H11F4NO2
Molecular Weight349.28 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentF-containing
Nitrogen Atoms1

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