(E)-3-(2-(4-chlorophenyl)thiazol-5-yl)-3-oxopropanal O-methyl oxime CAS 339279-40-2

Purity 97%+In StockPharmaceutical Standards
CAS No.339279-40-2
Molecular FormulaC13H11ClN2O2S
Molecular Weight294.76 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-3-(2-(4-chlorophenyl)thiazol-5-yl)-3-oxopropanal O-methyl oxime CAS 339279-40-2 chemical structure

Description

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.

(E)-3-(2-(4-chlorophenyl)thiazol-5-yl)-3-oxopropanal O-methyl oxime (CAS 339279-40-2) is a high-purity analytical reference standard with the molecular formula C13H11ClN2O2S and a molecular weight of 294.76 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution, (E)-3-(2-(4-chlorophenyl)thiazol-5-yl)-3-oxopropanal O-methyl oxime is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 294.76 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

As a certified reference material (CRM), (E)-3-(2-(4-chlorophenyl)thiazol-5-yl)-3-oxopropanal O-methyl oxime 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 FormulaC13H11ClN2O2S
Molecular Weight294.76 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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