4-Chloro-3-((4-fluorobenzyl)oxy)thiophene-2-carboxylic acid CAS 1710661-43-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1710661-43-0
Molecular FormulaC12H8ClFO3S
Molecular Weight286.71 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-3-((4-fluorobenzyl)oxy)thiophene-2-carboxylic acid CAS 1710661-43-0 chemical structure

Description

Based on its molecular formula C12H8ClFO3S, 4-Chloro-3-((4-fluorobenzyl)oxy)thiophene-2-carboxylic acid contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 286.71 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 4-Chloro-3-((4-fluorobenzyl)oxy)thiophene-2-carboxylic acid (CAS 1710661-43-0), a certified reference material (molecular formula C12H8ClFO3S, MW 286.71 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 4-Chloro-3-((4-fluorobenzyl)oxy)thiophene-2-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 FormulaC12H8ClFO3S
Molecular Weight286.71 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 chloroform, dichloromethane, ethyl acetate, 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Halogen ContentF/Cl-containing
Sulfur Atoms1

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