2-(4-Bromobenzyl)thiazole-4-carboxylic acid CAS 1086380-12-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1086380-12-2
Molecular FormulaC11H8BrNO2S
Molecular Weight298.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Bromobenzyl)thiazole-4-carboxylic acid CAS 1086380-12-2 chemical structure

Description

CATO supplies 2-(4-Bromobenzyl)thiazole-4-carboxylic acid (CAS 1086380-12-2), a certified reference material (molecular formula C11H8BrNO2S, MW 298.16 g/mol) for analytical method development and quality control.

Based on its molecular formula C11H8BrNO2S, 2-(4-Bromobenzyl)thiazole-4-carboxylic acid contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 298.16 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

CATO manufactures 2-(4-Bromobenzyl)thiazole-4-carboxylic 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 FormulaC11H8BrNO2S
Molecular Weight298.16 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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 ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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