3-Chloro-4-((4-chlorophenyl)thio)tetrahydrothiophene 1,1-dioxide CAS 13894-16-1

Purity 97%+In StockPharmaceutical Standards
CAS No.13894-16-1
Molecular FormulaC10H10Cl2O2S2
Molecular Weight297.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Chloro-4-((4-chlorophenyl)thio)tetrahydrothiophene 1,1-dioxide CAS 13894-16-1 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 3-Chloro-4-((4-chlorophenyl)thio)tetrahydrothiophene 1,1-dioxide (CAS 13894-16-1), a certified reference material (molecular formula C10H10Cl2O2S2, MW 297.22 g/mol) for analytical method development and quality control.

3-Chloro-4-((4-chlorophenyl)thio)tetrahydrothiophene 1,1-dioxide (C10H10Cl2O2S2) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO manufactures 3-Chloro-4-((4-chlorophenyl)thio)tetrahydrothiophene 1,1-dioxide 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 FormulaC10H10Cl2O2S2
Molecular Weight297.22 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; 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.)1960
Halogen ContentCl-containing
Sulfur Atoms2

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