Ethyl 4-(4-bromo-2-methylphenyl)thiazole-2-carboxylate CAS 886366-60-5

Purity 97%+In StockPharmaceutical Standards
CAS No.886366-60-5
Molecular FormulaC13H12BrNO2S
Molecular Weight326.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 4-(4-bromo-2-methylphenyl)thiazole-2-carboxylate CAS 886366-60-5 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 326.21 g/mol gives Ethyl 4-(4-bromo-2-methylphenyl)thiazole-2-carboxylate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Ethyl 4-(4-bromo-2-methylphenyl)thiazole-2-carboxylate (CAS 886366-60-5), molecular formula C13H12BrNO2S and molecular weight 326.21 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of Ethyl 4-(4-bromo-2-methylphenyl)thiazole-2-carboxylate (C13H12BrNO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.

As a certified reference material (CRM), Ethyl 4-(4-bromo-2-methylphenyl)thiazole-2-carboxylate 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.

Physical & Chemical Properties

Molecular FormulaC13H12BrNO2S
Molecular Weight326.21 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.)1987
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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