6-(Furan-2-yl)-3-phenylisoxazolo[5,4-b]pyridine-4-carboxylic acid CAS 937597-65-4

Purity 97%+In StockPharmaceutical Standards
CAS No.937597-65-4
Molecular FormulaC17H10N2O4
Molecular Weight306.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(Furan-2-yl)-3-phenylisoxazolo[5,4-b]pyridine-4-carboxylic acid CAS 937597-65-4 chemical structure

Description

Structurally, 6-(Furan-2-yl)-3-phenylisoxazolo[5,4-b]pyridine-4-carboxylic acid (C17H10N2O4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 14.0, corresponding to approximately 14 ring(s) or double-bond equivalent(s). With a molecular weight of 306.27 g/mol, it falls into the moderately-high-molecular-weight range. 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-(Furan-2-yl)-3-phenylisoxazolo[5,4-b]pyridine-4-carboxylic acid (CAS 937597-65-4), a certified reference material (molecular formula C17H10N2O4, MW 306.27 g/mol) for analytical method development and quality control.

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), 6-(Furan-2-yl)-3-phenylisoxazolo[5,4-b]pyridine-4-carboxylic acid 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 FormulaC17H10N2O4
Molecular Weight306.27 g/mol
AppearancePale yellow to 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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2

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