N-(3,5-dichlorophenyl)-3-(4-methoxyphenyl)isoxazole-5-carboxamide CAS 477859-14-6

Purity 97%+In StockPharmaceutical Standards
CAS No.477859-14-6
Molecular FormulaC17H12Cl2N2O3
Molecular Weight363.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3,5-dichlorophenyl)-3-(4-methoxyphenyl)isoxazole-5-carboxamide CAS 477859-14-6 chemical structure

Description

Based on its molecular formula C17H12Cl2N2O3, N-(3,5-dichlorophenyl)-3-(4-methoxyphenyl)isoxazole-5-carboxamide contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 363.19 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

N-(3,5-dichlorophenyl)-3-(4-methoxyphenyl)isoxazole-5-carboxamide (CAS 477859-14-6), molecular formula C17H12Cl2N2O3 and molecular weight 363.19 g/mol, is a CATO reference standard with documented purity and traceability.

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

As a certified reference material (CRM), N-(3,5-dichlorophenyl)-3-(4-methoxyphenyl)isoxazole-5-carboxamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC17H12Cl2N2O3
Molecular Weight363.19 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; 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.)2025
Halogen ContentCl-containing
Nitrogen Atoms2

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