2-(4-bromothiophen-2-yl)-1,3-thiazole-4-carboxylic acid CAS 1094456-15-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1094456-15-1
Molecular FormulaC8H4BrNO2S2
Molecular Weight290.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-bromothiophen-2-yl)-1,3-thiazole-4-carboxylic acid CAS 1094456-15-1 chemical structure

Description

CATO supplies 2-(4-bromothiophen-2-yl)-1,3-thiazole-4-carboxylic acid (CAS 1094456-15-1), a certified reference material (molecular formula C8H4BrNO2S2, MW 290.16 g/mol) for analytical method development and quality control.

Based on its molecular formula C8H4BrNO2S2, 2-(4-bromothiophen-2-yl)-1,3-thiazole-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 290.16 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 2-(4-bromothiophen-2-yl)-1,3-thiazole-4-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 FormulaC8H4BrNO2S2
Molecular Weight290.16 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms2

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