N-[2-(1H-Indol-3-yl)ethyl]-5-methyl-3-phenyl-1,2-oxazole-4-carboxamide CAS 851905-89-0

Purity 97%+In StockPharmaceutical Standards
CAS No.851905-89-0
Molecular FormulaC21H19N3O2
Molecular Weight345.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-[2-(1H-Indol-3-yl)ethyl]-5-methyl-3-phenyl-1,2-oxazole-4-carboxamide CAS 851905-89-0 chemical structure

Description

CATO manufactures N-[2-(1H-Indol-3-yl)ethyl]-5-methyl-3-phenyl-1,2-oxazole-4-carboxamide 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 N-[2-(1H-Indol-3-yl)ethyl]-5-methyl-3-phenyl-1,2-oxazole-4-carboxamide (CAS 851905-89-0), a certified reference material (molecular formula C21H19N3O2, MW 345.39 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, N-[2-(1H-Indol-3-yl)ethyl]-5-methyl-3-phenyl-1,2-oxazole-4-carboxamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 345.39 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 FormulaC21H19N3O2
Molecular Weight345.39 g/mol
AppearancePale yellow to yellow crystalline powder
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
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms3

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