4-(3-Fluorophenyl)-1,2,3-thiadiazole-5-carboxylic acid CAS 1495844-95-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1495844-95-5
Molecular FormulaC9H5FN2O2S
Molecular Weight224.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(3-Fluorophenyl)-1,2,3-thiadiazole-5-carboxylic acid CAS 1495844-95-5 chemical structure

Description

Based on its molecular formula C9H5FN2O2S, 4-(3-Fluorophenyl)-1,2,3-thiadiazole-5-carboxylic acid contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 224.21 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

4-(3-Fluorophenyl)-1,2,3-thiadiazole-5-carboxylic acid (CAS 1495844-95-5), molecular formula C9H5FN2O2S and molecular weight 224.21 g/mol, is a CATO reference standard with documented purity and traceability.

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

As a certified reference material (CRM), 4-(3-Fluorophenyl)-1,2,3-thiadiazole-5-carboxylic acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC9H5FN2O2S
Molecular Weight224.21 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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