6-bromo-2-[(E)-2-(thiophen-2-yl)ethenyl]quinoline-4-carboxylic acid CAS 926193-00-2

Purity 97%+In StockPharmaceutical Standards
CAS No.926193-00-2
Molecular FormulaC16H10BrNO2S
Molecular Weight360.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-bromo-2-[(E)-2-(thiophen-2-yl)ethenyl]quinoline-4-carboxylic acid CAS 926193-00-2 chemical structure

Description

6-bromo-2-[(E)-2-(thiophen-2-yl)ethenyl]quinoline-4-carboxylic acid (CAS 926193-00-2), molecular formula C16H10BrNO2S and molecular weight 360.23 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C16H10BrNO2S, 6-bromo-2-[(E)-2-(thiophen-2-yl)ethenyl]quinoline-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 360.23 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

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 FormulaC16H10BrNO2S
Molecular Weight360.23 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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