N-(5-iodo-3-methylpyridin-2-yl)-4-(trifluoromethyl)benzamide CAS 477889-92-2

Purity 97%+In StockPharmaceutical Standards
CAS No.477889-92-2
Molecular FormulaC14H10F3IN2O
Molecular Weight406.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(5-iodo-3-methylpyridin-2-yl)-4-(trifluoromethyl)benzamide CAS 477889-92-2 chemical structure

Description

N-(5-iodo-3-methylpyridin-2-yl)-4-(trifluoromethyl)benzamide (CAS 477889-92-2), molecular formula C14H10F3IN2O and molecular weight 406.14 g/mol, is a CATO reference standard with documented purity and traceability.

N-(5-iodo-3-methylpyridin-2-yl)-4-(trifluoromethyl)benzamide (C14H10F3IN2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/iodine 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.

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 FormulaC14H10F3IN2O
Molecular Weight406.14 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF/I-containing
Nitrogen Atoms2

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