2-[(2-Fluorobenzoyl)amino]-1,3-thiazole-4-carboxylic acid CAS 941869-55-2

Purity 97%+In StockPharmaceutical Standards
CAS No.941869-55-2
Molecular FormulaC11H7FN2O3S
Molecular Weight266.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[(2-Fluorobenzoyl)amino]-1,3-thiazole-4-carboxylic acid CAS 941869-55-2 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.

CATO supplies 2-[(2-Fluorobenzoyl)amino]-1,3-thiazole-4-carboxylic acid (CAS 941869-55-2), a certified reference material (molecular formula C11H7FN2O3S, MW 266.25 g/mol) for analytical method development and quality control.

Structurally, 2-[(2-Fluorobenzoyl)amino]-1,3-thiazole-4-carboxylic acid (C11H7FN2O3S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 266.25 g/mol, it falls into the medium-molecular-weight range. 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).

CATO manufactures 2-[(2-Fluorobenzoyl)amino]-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 FormulaC11H7FN2O3S
Molecular Weight266.25 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 methanol, ethanol, 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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