6-amino-7-fluoro-2H,3H,4H-pyrido[3,2-b][1,4]oxazin-3-one CAS 1909347-79-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1909347-79-0
Molecular FormulaC7H6FN3O2
Molecular Weight183.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-amino-7-fluoro-2H,3H,4H-pyrido[3,2-b][1,4]oxazin-3-one CAS 1909347-79-0 chemical structure

Description

CATO supplies 6-amino-7-fluoro-2H,3H,4H-pyrido[3,2-b][1,4]oxazin-3-one (CAS 1909347-79-0), a certified reference material (molecular formula C7H6FN3O2, MW 183.14 g/mol) for analytical method development and quality control.

The molecular framework of 6-amino-7-fluoro-2H,3H,4H-pyrido[3,2-b][1,4]oxazin-3-one (C7H6FN3O2) is characterized by an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC7H6FN3O2
Molecular Weight183.14 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, 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; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentF-containing
Nitrogen Atoms3

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