6-amino-2-(4-methoxyphenyl)pyrimidin-4(3H)-one CAS 1154345-57-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1154345-57-9
Molecular FormulaC11H15N3O2
Molecular Weight221.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-amino-2-(4-methoxyphenyl)pyrimidin-4(3H)-one CAS 1154345-57-9 chemical structure

Description

Based on its molecular formula C11H15N3O2, 6-amino-2-(4-methoxyphenyl)pyrimidin-4(3H)-one contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 221.26 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 6-amino-2-(4-methoxyphenyl)pyrimidin-4(3H)-one (CAS 1154345-57-9), a certified reference material (molecular formula C11H15N3O2, MW 221.26 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.

As a certified reference material (CRM), 6-amino-2-(4-methoxyphenyl)pyrimidin-4(3H)-one 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 FormulaC11H15N3O2
Molecular Weight221.26 g/mol
AppearanceOff-white to pale yellow crystalline powder
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
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms3

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