2-[2-(3-fluorophenyl)-1,3-thiazol-4-yl]acetic acid CAS 794554-74-8

Purity 97%+In StockPharmaceutical Standards
CAS No.794554-74-8
Molecular FormulaC11H8FNO2S
Molecular Weight237.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[2-(3-fluorophenyl)-1,3-thiazol-4-yl]acetic acid CAS 794554-74-8 chemical structure

Description

The molecular framework of 2-[2-(3-fluorophenyl)-1,3-thiazol-4-yl]acetic acid (C11H8FNO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 supplies 2-[2-(3-fluorophenyl)-1,3-thiazol-4-yl]acetic acid (CAS 794554-74-8), a certified reference material (molecular formula C11H8FNO2S, MW 237.25 g/mol) for analytical method development and quality control.

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-[2-(3-fluorophenyl)-1,3-thiazol-4-yl]acetic 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 FormulaC11H8FNO2S
Molecular Weight237.25 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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