ethyl 7-bromo-4-oxo-pyrido[1,2-a]pyrimidine-3-carboxylate CAS 16867-56-4

Purity 97%+In StockPharmaceutical Standards
CAS No.16867-56-4
Molecular FormulaC11H17BrN2O3
Molecular Weight305.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

ethyl 7-bromo-4-oxo-pyrido[1,2-a]pyrimidine-3-carboxylate CAS 16867-56-4 chemical structure

Description

ethyl 7-bromo-4-oxo-pyrido[1,2-a]pyrimidine-3-carboxylate (C11H17BrN2O3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; 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).

CATO supplies ethyl 7-bromo-4-oxo-pyrido[1,2-a]pyrimidine-3-carboxylate (CAS 16867-56-4), a certified reference material (molecular formula C11H17BrN2O3, MW 305.17 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 ethyl 7-bromo-4-oxo-pyrido[1,2-a]pyrimidine-3-carboxylate 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 FormulaC11H17BrN2O3
Molecular Weight305.17 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Halogen ContentBr-containing
Nitrogen Atoms2

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