1-(3-Bromophenyl)-3,3-bis(methylsulfanyl)prop-2-en-1-one CAS 71504-03-5

Purity 97%+In StockPharmaceutical Standards
CAS No.71504-03-5
Molecular FormulaC11H11BrOS2
Molecular Weight303.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(3-Bromophenyl)-3,3-bis(methylsulfanyl)prop-2-en-1-one CAS 71504-03-5 chemical structure

Description

The occurrence of 1-(3-Bromophenyl)-3,3-bis(methylsulfanyl)prop-2-en-1-one is closely related to sulfur-containing functionality, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 1-(3-Bromophenyl)-3,3-bis(methylsulfanyl)prop-2-en-1-one (CAS 71504-03-5), a certified reference material (molecular formula C11H11BrOS2, MW 303.24 g/mol) for analytical method development and quality control.

1-(3-Bromophenyl)-3,3-bis(methylsulfanyl)prop-2-en-1-one (C11H11BrOS2) contains sulfur-containing functionality, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; 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.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC11H11BrOS2
Molecular Weight303.24 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1977
Halogen ContentBr-containing
Sulfur Atoms2

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