3-Bromo-N-(4-methoxyphenyl)thiophene-2-carboxamide CAS 88791-39-3

Purity 97%+In StockPharmaceutical Standards
CAS No.88791-39-3
Molecular FormulaC12H10BrNO2S
Molecular Weight312.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Bromo-N-(4-methoxyphenyl)thiophene-2-carboxamide CAS 88791-39-3 chemical structure

Description

CATO manufactures 3-Bromo-N-(4-methoxyphenyl)thiophene-2-carboxamide 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.

3-Bromo-N-(4-methoxyphenyl)thiophene-2-carboxamide (CAS 88791-39-3) is a high-purity analytical reference standard with the molecular formula C12H10BrNO2S and a molecular weight of 312.18 g/mol.

3-Bromo-N-(4-methoxyphenyl)thiophene-2-carboxamide (C12H10BrNO2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

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.

Physical & Chemical Properties

Molecular FormulaC12H10BrNO2S
Molecular Weight312.18 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.)1982
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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