(E)-3-(4-(tert-butyl)phenyl)-N-(2,4-difluorophenyl)acrylamide CAS 298215-24-4

Purity 97%+In StockPharmaceutical Standards
CAS No.298215-24-4
Molecular FormulaC19H19F2NO
Molecular Weight315.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-3-(4-(tert-butyl)phenyl)-N-(2,4-difluorophenyl)acrylamide CAS 298215-24-4 chemical structure

Description

CATO manufactures (E)-3-(4-(tert-butyl)phenyl)-N-(2,4-difluorophenyl)acrylamide 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.

CATO supplies (E)-3-(4-(tert-butyl)phenyl)-N-(2,4-difluorophenyl)acrylamide (CAS 298215-24-4), a certified reference material (molecular formula C19H19F2NO, MW 315.36 g/mol) for analytical method development and quality control.

(E)-3-(4-(tert-butyl)phenyl)-N-(2,4-difluorophenyl)acrylamide (C19H19F2NO) contains a steroid core, an amide 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; 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.

Physical & Chemical Properties

Molecular FormulaC19H19F2NO
Molecular Weight315.36 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1

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