2-Bromo-5-chloro-1,3-thiazole-4-carboxylic acid CAS 1027169-53-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1027169-53-4
Molecular FormulaC4HBrClNO2S
Molecular Weight242.48 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Bromo-5-chloro-1,3-thiazole-4-carboxylic acid CAS 1027169-53-4 chemical structure

Description

Based on its molecular formula C4HBrClNO2S, 2-Bromo-5-chloro-1,3-thiazole-4-carboxylic acid contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine/bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 242.48 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

2-Bromo-5-chloro-1,3-thiazole-4-carboxylic acid (CAS 1027169-53-4) is a high-purity analytical reference standard with the molecular formula C4HBrClNO2S and a molecular weight of 242.48 g/mol.

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-Bromo-5-chloro-1,3-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 FormulaC4HBrClNO2S
Molecular Weight242.48 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)4.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1988
Halogen ContentCl/Br-containing
Nitrogen Atoms1
Sulfur Atoms1

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