N-(3-methoxypropyl)-4-(3-(trifluoromethyl)benzoyl)-1H-pyrrole-2-carboxamide CAS 478064-59-4

Purity 97%+In StockPharmaceutical Standards
CAS No.478064-59-4
Molecular FormulaC17H17F3N2O3
Molecular Weight354.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-methoxypropyl)-4-(3-(trifluoromethyl)benzoyl)-1H-pyrrole-2-carboxamide CAS 478064-59-4 chemical structure

Description

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

N-(3-methoxypropyl)-4-(3-(trifluoromethyl)benzoyl)-1H-pyrrole-2-carboxamide (CAS 478064-59-4), molecular formula C17H17F3N2O3 and molecular weight 354.32 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution, N-(3-methoxypropyl)-4-(3-(trifluoromethyl)benzoyl)-1H-pyrrole-2-carboxamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 354.32 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures N-(3-methoxypropyl)-4-(3-(trifluoromethyl)benzoyl)-1H-pyrrole-2-carboxamide 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.

Physical & Chemical Properties

Molecular FormulaC17H17F3N2O3
Molecular Weight354.32 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2

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