(E)-4-(3-(thiophen-2-yl)acryloyl)phenyl 4-fluorobenzenesulfonate CAS 297150-17-5

Purity 97%+In StockPharmaceutical Standards
CAS No.297150-17-5
Molecular FormulaC19H13FO4S2
Molecular Weight388.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-4-(3-(thiophen-2-yl)acryloyl)phenyl 4-fluorobenzenesulfonate CAS 297150-17-5 chemical structure

Description

(E)-4-(3-(thiophen-2-yl)acryloyl)phenyl 4-fluorobenzenesulfonate (C19H13FO4S2) contains a flavonoid core, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. 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. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO supplies (E)-4-(3-(thiophen-2-yl)acryloyl)phenyl 4-fluorobenzenesulfonate (CAS 297150-17-5), a certified reference material (molecular formula C19H13FO4S2, MW 388.43 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), (E)-4-(3-(thiophen-2-yl)acryloyl)phenyl 4-fluorobenzenesulfonate 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 FormulaC19H13FO4S2
Molecular Weight388.43 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Sulfur Atoms2

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