3-(4-Bromophenoxy)tetrahydrothiophene 1,1-dioxide CAS 53583-33-8

Purity 97%+In StockPharmaceutical Standards
CAS No.53583-33-8
Molecular FormulaC10H11BrO3S
Molecular Weight291.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Bromophenoxy)tetrahydrothiophene 1,1-dioxide CAS 53583-33-8 chemical structure

Description

Based on its molecular formula C10H11BrO3S, 3-(4-Bromophenoxy)tetrahydrothiophene 1,1-dioxide contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 291.16 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 3-(4-Bromophenoxy)tetrahydrothiophene 1,1-dioxide (CAS 53583-33-8), a certified reference material (molecular formula C10H11BrO3S, MW 291.16 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 3-(4-Bromophenoxy)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 FormulaC10H11BrO3S
Molecular Weight291.16 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.)1972
Halogen ContentBr-containing
Sulfur Atoms1

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