2-(3-Bromophenyl)-4-methylthiazole-5-carboxylic acid CAS 927974-39-8

Purity 97%+In StockPharmaceutical Standards
CAS No.927974-39-8
Molecular FormulaC11H8BrNO2S
Molecular Weight298.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3-Bromophenyl)-4-methylthiazole-5-carboxylic acid CAS 927974-39-8 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 2-(3-Bromophenyl)-4-methylthiazole-5-carboxylic acid.

CATO supplies 2-(3-Bromophenyl)-4-methylthiazole-5-carboxylic acid (CAS 927974-39-8), 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-(3-Bromophenyl)-4-methylthiazole-5-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).

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

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.)1987
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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