6-(3-methoxyphenyl)-3-methylisoxazolo[5,4-b]pyridine-4-carboxylic acid CAS 1011389-03-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1011389-03-9
Molecular FormulaC15H12N2O4
Molecular Weight284.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(3-methoxyphenyl)-3-methylisoxazolo[5,4-b]pyridine-4-carboxylic acid CAS 1011389-03-9 chemical structure

Description

CATO supplies 6-(3-methoxyphenyl)-3-methylisoxazolo[5,4-b]pyridine-4-carboxylic acid (CAS 1011389-03-9), a certified reference material (molecular formula C15H12N2O4, MW 284.27 g/mol) for analytical method development and quality control.

Structurally, 6-(3-methoxyphenyl)-3-methylisoxazolo[5,4-b]pyridine-4-carboxylic acid (C15H12N2O4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 11.0, corresponding to approximately 11 ring(s) or double-bond equivalent(s). With a molecular weight of 284.27 g/mol, it falls into the medium-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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-(3-methoxyphenyl)-3-methylisoxazolo[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 FormulaC15H12N2O4
Molecular Weight284.27 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms2

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