2-Methyl-N-phenylimidazo[1,2-a]pyrimidine-3-carboxamide CAS 62772-76-3

Purity 97%+In StockPharmaceutical Standards
CAS No.62772-76-3
Molecular FormulaC14H12N4O
Molecular Weight252.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Methyl-N-phenylimidazo[1,2-a]pyrimidine-3-carboxamide CAS 62772-76-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 252.27 g/mol gives 2-Methyl-N-phenylimidazo[1,2-a]pyrimidine-3-carboxamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

2-Methyl-N-phenylimidazo[1,2-a]pyrimidine-3-carboxamide (CAS 62772-76-3) is a high-purity analytical reference standard with the molecular formula C14H12N4O and a molecular weight of 252.27 g/mol.

2-Methyl-N-phenylimidazo[1,2-a]pyrimidine-3-carboxamide (C14H12N4O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its physicochemical properties are representative of its class; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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), 2-Methyl-N-phenylimidazo[1,2-a]pyrimidine-3-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 FormulaC14H12N4O
Molecular Weight252.27 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Nitrogen Atoms4

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