Methyl 4-(4-((3-chloropropanoyl)oxy)-5-methylthiazol-2-yl)benzoate CAS 338409-54-4

Purity 97%+In StockPharmaceutical Standards
CAS No.338409-54-4
Molecular FormulaC15H14ClNO4S
Molecular Weight339.79 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 4-(4-((3-chloropropanoyl)oxy)-5-methylthiazol-2-yl)benzoate CAS 338409-54-4 chemical structure

Description

CATO supplies Methyl 4-(4-((3-chloropropanoyl)oxy)-5-methylthiazol-2-yl)benzoate (CAS 338409-54-4), a certified reference material (molecular formula C15H14ClNO4S, MW 339.79 g/mol) for analytical method development and quality control.

The molecular framework of Methyl 4-(4-((3-chloropropanoyl)oxy)-5-methylthiazol-2-yl)benzoate (C15H14ClNO4S) is characterized by a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

As a certified reference material (CRM), Methyl 4-(4-((3-chloropropanoyl)oxy)-5-methylthiazol-2-yl)benzoate 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 FormulaC15H14ClNO4S
Molecular Weight339.79 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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