1-Methyl-4-phenyl-1h-pyrazolo[3,4-b]pyridine-3-carboxylic acid CAS 1354706-24-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1354706-24-3
Molecular FormulaC14H11N3O2
Molecular Weight253.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Methyl-4-phenyl-1h-pyrazolo[3,4-b]pyridine-3-carboxylic acid CAS 1354706-24-3 chemical structure

Description

The molecular framework of 1-Methyl-4-phenyl-1h-pyrazolo[3,4-b]pyridine-3-carboxylic acid (C14H11N3O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 1-Methyl-4-phenyl-1h-pyrazolo[3,4-b]pyridine-3-carboxylic acid (CAS 1354706-24-3), a certified reference material (molecular formula C14H11N3O2, MW 253.26 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.

CATO manufactures 1-Methyl-4-phenyl-1h-pyrazolo[3,4-b]pyridine-3-carboxylic acid 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 FormulaC14H11N3O2
Molecular Weight253.26 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.)1991
Nitrogen Atoms3

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