3-bromoimidazo[5,1-b]thiazole-7-carboxylic acid CAS 1352898-75-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1352898-75-9
Molecular FormulaC6H3BrN2O2S
Molecular Weight247.07 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-bromoimidazo[5,1-b]thiazole-7-carboxylic acid CAS 1352898-75-9 chemical structure

Description

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

3-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (CAS 1352898-75-9) is a high-purity analytical reference standard with the molecular formula C6H3BrN2O2S and a molecular weight of 247.07 g/mol.

Owing to an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system, 3-bromoimidazo[5,1-b]thiazole-7-carboxylic acid is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 247.07 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO manufactures 3-bromoimidazo[5,1-b]thiazole-7-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 FormulaC6H3BrN2O2S
Molecular Weight247.07 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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