2-Bromo-5-(4-fluorophenyl)thiazole-4-carboxylic acid CAS 1137129-05-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1137129-05-5
Molecular FormulaC10H5BrFNO2S
Molecular Weight302.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Bromo-5-(4-fluorophenyl)thiazole-4-carboxylic acid CAS 1137129-05-5 chemical structure

Description

As a certified reference material (CRM), 2-Bromo-5-(4-fluorophenyl)thiazole-4-carboxylic acid 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.

CATO supplies 2-Bromo-5-(4-fluorophenyl)thiazole-4-carboxylic acid (CAS 1137129-05-5), a certified reference material (molecular formula C10H5BrFNO2S, MW 302.12 g/mol) for analytical method development and quality control.

Based on its molecular formula C10H5BrFNO2S, 2-Bromo-5-(4-fluorophenyl)thiazole-4-carboxylic acid contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 302.12 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC10H5BrFNO2S
Molecular Weight302.12 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.)1989
Halogen ContentF/Br-containing
Nitrogen Atoms1
Sulfur Atoms1

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