8-Methoxy-N-(4-methylthiazol-2-yl)-2-oxo-2H-chromene-3-carboxamide CAS 484022-70-0

Purity 97%+In StockPharmaceutical Standards
CAS No.484022-70-0
Molecular FormulaC15H12N2O4S
Molecular Weight316.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

8-Methoxy-N-(4-methylthiazol-2-yl)-2-oxo-2H-chromene-3-carboxamide CAS 484022-70-0 chemical structure

Description

CATO manufactures 8-Methoxy-N-(4-methylthiazol-2-yl)-2-oxo-2H-chromene-3-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 8-Methoxy-N-(4-methylthiazol-2-yl)-2-oxo-2H-chromene-3-carboxamide (CAS 484022-70-0), a certified reference material (molecular formula C15H12N2O4S, MW 316.33 g/mol) for analytical method development and quality control.

Structurally, 8-Methoxy-N-(4-methylthiazol-2-yl)-2-oxo-2H-chromene-3-carboxamide (C15H12N2O4S) contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 11.0, corresponding to approximately 11 ring(s) or double-bond equivalent(s). With a molecular weight of 316.33 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC15H12N2O4S
Molecular Weight316.33 g/mol
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms2
Sulfur Atoms1

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