3-[(3-fluorophenyl)sulfanyl]-2-hydroxy-2-methylpropanoic acid CAS 1506047-42-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1506047-42-2
Molecular FormulaC10H11FO3S
Molecular Weight230.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[(3-fluorophenyl)sulfanyl]-2-hydroxy-2-methylpropanoic acid CAS 1506047-42-2 chemical structure

Description

Owing to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system, 3-[(3-fluorophenyl)sulfanyl]-2-hydroxy-2-methylpropanoic acid is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 230.26 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

3-[(3-fluorophenyl)sulfanyl]-2-hydroxy-2-methylpropanoic acid (CAS 1506047-42-2), molecular formula C10H11FO3S and molecular weight 230.26 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), 3-[(3-fluorophenyl)sulfanyl]-2-hydroxy-2-methylpropanoic 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 FormulaC10H11FO3S
Molecular Weight230.26 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentF-containing
Sulfur Atoms1

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