2-(4-Fluorophenyl)furo[2,3-b]quinoxaline CAS 922145-30-0

Purity 97%+In StockPharmaceutical Standards
CAS No.922145-30-0
Molecular FormulaC16H9FN2O
Molecular Weight264.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Fluorophenyl)furo[2,3-b]quinoxaline CAS 922145-30-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 264.25 g/mol gives 2-(4-Fluorophenyl)furo[2,3-b]quinoxaline distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

2-(4-Fluorophenyl)furo[2,3-b]quinoxaline (CAS 922145-30-0) is a high-purity analytical reference standard with the molecular formula C16H9FN2O and a molecular weight of 264.25 g/mol.

Based on its molecular formula C16H9FN2O, 2-(4-Fluorophenyl)furo[2,3-b]quinoxaline contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 264.25 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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

As a certified reference material (CRM), 2-(4-Fluorophenyl)furo[2,3-b]quinoxaline 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 FormulaC16H9FN2O
Molecular Weight264.25 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, 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
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms2

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