4-[(5-bromothiophen-2-yl)methoxy]-3-methoxybenzoic acid CAS 1016705-48-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1016705-48-8
Molecular FormulaC13H11BrO4S
Molecular Weight343.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-[(5-bromothiophen-2-yl)methoxy]-3-methoxybenzoic acid CAS 1016705-48-8 chemical structure

Description

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.

4-[(5-bromothiophen-2-yl)methoxy]-3-methoxybenzoic acid (CAS 1016705-48-8) is a high-purity analytical reference standard with the molecular formula C13H11BrO4S and a molecular weight of 343.19 g/mol.

4-[(5-bromothiophen-2-yl)methoxy]-3-methoxybenzoic acid (C13H11BrO4S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system. It is notably hygroscopic, 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 4-[(5-bromothiophen-2-yl)methoxy]-3-methoxybenzoic 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 FormulaC13H11BrO4S
Molecular Weight343.19 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; 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.)1988
Halogen ContentBr-containing
Sulfur Atoms1

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