4-((2-((2-Fluorophenyl)amino)-4-oxothiazol-5(4H)-ylidene)methyl)benzoic acid CAS 494191-73-0

Purity 97%+In StockPharmaceutical Standards
CAS No.494191-73-0
Molecular FormulaC17H11FN2O3S
Molecular Weight342.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-((2-((2-Fluorophenyl)amino)-4-oxothiazol-5(4H)-ylidene)methyl)benzoic acid CAS 494191-73-0 chemical structure

Description

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

CATO supplies 4-((2-((2-Fluorophenyl)amino)-4-oxothiazol-5(4H)-ylidene)methyl)benzoic acid (CAS 494191-73-0), a certified reference material (molecular formula C17H11FN2O3S, MW 342.34 g/mol) for analytical method development and quality control.

4-((2-((2-Fluorophenyl)amino)-4-oxothiazol-5(4H)-ylidene)methyl)benzoic acid (C17H11FN2O3S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures 4-((2-((2-Fluorophenyl)amino)-4-oxothiazol-5(4H)-ylidene)methyl)benzoic acid 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.

Physical & Chemical Properties

Molecular FormulaC17H11FN2O3S
Molecular Weight342.34 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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