4-(3-Chlorophenyl)tetrahydro-2h-thiopyran-4-carboxylic acid 1,1-dioxide CAS 2490704-92-0

Purity 97%+In StockPharmaceutical Standards
CAS No.2490704-92-0
Molecular FormulaC12H13ClO4S
Molecular Weight288.75 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(3-Chlorophenyl)tetrahydro-2h-thiopyran-4-carboxylic acid 1,1-dioxide CAS 2490704-92-0 chemical structure

Description

As a certified reference material (CRM), 4-(3-Chlorophenyl)tetrahydro-2h-thiopyran-4-carboxylic acid 1,1-dioxide 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.

4-(3-Chlorophenyl)tetrahydro-2h-thiopyran-4-carboxylic acid 1,1-dioxide (CAS 2490704-92-0), molecular formula C12H13ClO4S and molecular weight 288.75 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system, 4-(3-Chlorophenyl)tetrahydro-2h-thiopyran-4-carboxylic acid 1,1-dioxide is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 288.75 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.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC12H13ClO4S
Molecular Weight288.75 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2000
Halogen ContentCl-containing
Sulfur Atoms1

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