(Z)-4-(3-Bromo-4-methoxybenzylidene)-2-(methylthio)thiazol-5(4H)-one CAS 430464-08-7

Purity 97%+In StockPharmaceutical Standards
CAS No.430464-08-7
Molecular FormulaC12H10BrNO2S2
Molecular Weight344.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(Z)-4-(3-Bromo-4-methoxybenzylidene)-2-(methylthio)thiazol-5(4H)-one CAS 430464-08-7 chemical structure

Description

As a certified reference material (CRM), (Z)-4-(3-Bromo-4-methoxybenzylidene)-2-(methylthio)thiazol-5(4H)-one 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.

(Z)-4-(3-Bromo-4-methoxybenzylidene)-2-(methylthio)thiazol-5(4H)-one (CAS 430464-08-7), molecular formula C12H10BrNO2S2 and molecular weight 344.25 g/mol, is a CATO reference standard with documented purity and traceability.

(Z)-4-(3-Bromo-4-methoxybenzylidene)-2-(methylthio)thiazol-5(4H)-one (C12H10BrNO2S2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

Physical & Chemical Properties

Molecular FormulaC12H10BrNO2S2
Molecular Weight344.25 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms2

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