3-({[3,5-bis(trifluoromethyl)phenyl]thio}methyl)-2,5-dichlorothiophene CAS 648408-58-6

Purity 97%+In StockPharmaceutical Standards
CAS No.648408-58-6
Molecular FormulaC13H6Cl2F6S2
Molecular Weight411.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-({[3,5-bis(trifluoromethyl)phenyl]thio}methyl)-2,5-dichlorothiophene CAS 648408-58-6 chemical structure

Description

Based on its molecular formula C13H6Cl2F6S2, 3-({[3,5-bis(trifluoromethyl)phenyl]thio}methyl)-2,5-dichlorothiophene contains sulfur-containing functionality, fluorine/chlorine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 411.21 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies 3-({[3,5-bis(trifluoromethyl)phenyl]thio}methyl)-2,5-dichlorothiophene (CAS 648408-58-6), a certified reference material (molecular formula C13H6Cl2F6S2, MW 411.21 g/mol) for analytical method development and quality control.

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.

As a certified reference material (CRM), 3-({[3,5-bis(trifluoromethyl)phenyl]thio}methyl)-2,5-dichlorothiophene 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 FormulaC13H6Cl2F6S2
Molecular Weight411.21 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentF/Cl-containing
Sulfur Atoms2

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