N-(4-(1H-Pyrrol-1-yl)phenyl)-2,2,2-trifluoroacetamide CAS 1789466-57-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1789466-57-4
Molecular FormulaC12H9F3N2O
Molecular Weight254.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-(1H-Pyrrol-1-yl)phenyl)-2,2,2-trifluoroacetamide CAS 1789466-57-4 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution, N-(4-(1H-Pyrrol-1-yl)phenyl)-2,2,2-trifluoroacetamide is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 254.21 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 supplies N-(4-(1H-Pyrrol-1-yl)phenyl)-2,2,2-trifluoroacetamide (CAS 1789466-57-4), a certified reference material (molecular formula C12H9F3N2O, MW 254.21 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.

CATO manufactures N-(4-(1H-Pyrrol-1-yl)phenyl)-2,2,2-trifluoroacetamide 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 FormulaC12H9F3N2O
Molecular Weight254.21 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Halogen ContentF-containing
Nitrogen Atoms2

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