N-(3-Chlorophenyl)-6-phenyl-2-(pyridin-3-yl)pyrimidine-4-carboxamide CAS 860787-58-2

Purity 97%+In StockPharmaceutical Standards
CAS No.860787-58-2
Molecular FormulaC22H15ClN4O
Molecular Weight386.83 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Chlorophenyl)-6-phenyl-2-(pyridin-3-yl)pyrimidine-4-carboxamide CAS 860787-58-2 chemical structure

Description

The molecular framework of N-(3-Chlorophenyl)-6-phenyl-2-(pyridin-3-yl)pyrimidine-4-carboxamide (C22H15ClN4O) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

N-(3-Chlorophenyl)-6-phenyl-2-(pyridin-3-yl)pyrimidine-4-carboxamide (CAS 860787-58-2), molecular formula C22H15ClN4O and molecular weight 386.83 g/mol, is a CATO reference standard with documented purity and traceability.

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), N-(3-Chlorophenyl)-6-phenyl-2-(pyridin-3-yl)pyrimidine-4-carboxamide 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 FormulaC22H15ClN4O
Molecular Weight386.83 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, 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)17.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms4

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