5-(3,4-Dichlorophenyl)-3-{[3-(trifluoromethyl)phenoxy]methyl}-1,2-oxazole CAS 339019-85-1

Purity 97%+In StockPharmaceutical Standards
CAS No.339019-85-1
Molecular FormulaC17H10Cl2F3NO2
Molecular Weight388.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(3,4-Dichlorophenyl)-3-{[3-(trifluoromethyl)phenoxy]methyl}-1,2-oxazole CAS 339019-85-1 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 5-(3,4-Dichlorophenyl)-3-{[3-(trifluoromethyl)phenoxy]methyl}-1,2-oxazole (CAS 339019-85-1), a certified reference material (molecular formula C17H10Cl2F3NO2, MW 388.17 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, 5-(3,4-Dichlorophenyl)-3-{[3-(trifluoromethyl)phenoxy]methyl}-1,2-oxazole is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 388.17 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 5-(3,4-Dichlorophenyl)-3-{[3-(trifluoromethyl)phenoxy]methyl}-1,2-oxazole 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 FormulaC17H10Cl2F3NO2
Molecular Weight388.17 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF/Cl-containing
Nitrogen Atoms1

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