5-bromo-1-benzothiophene-3-carboxylic acid CAS 7312-24-5

Purity 97%+In StockPharmaceutical Standards
CAS No.7312-24-5
Molecular FormulaC9H13BrO2S
Molecular Weight265.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-bromo-1-benzothiophene-3-carboxylic acid CAS 7312-24-5 chemical structure

Description

5-bromo-1-benzothiophene-3-carboxylic acid (C9H13BrO2S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution. Halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

5-bromo-1-benzothiophene-3-carboxylic acid (CAS 7312-24-5) is a high-purity analytical reference standard with the molecular formula C9H13BrO2S and a molecular weight of 265.17 g/mol.

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

CATO manufactures 5-bromo-1-benzothiophene-3-carboxylic 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 FormulaC9H13BrO2S
Molecular Weight265.17 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1959
Halogen ContentBr-containing
Sulfur Atoms1

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