2-Phenyl-3H-pyrido[3,4-b][1,4]diazepin-4(5H)-one CAS 24188-36-1

Purity 97%+In StockPharmaceutical Standards
CAS No.24188-36-1
Molecular FormulaC14H11N3O
Molecular Weight237.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Phenyl-3H-pyrido[3,4-b][1,4]diazepin-4(5H)-one CAS 24188-36-1 chemical structure

Description

The occurrence of 2-Phenyl-3H-pyrido[3,4-b][1,4]diazepin-4(5H)-one is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 2-Phenyl-3H-pyrido[3,4-b][1,4]diazepin-4(5H)-one (CAS 24188-36-1), a certified reference material (molecular formula C14H11N3O, MW 237.26 g/mol) for analytical method development and quality control.

The molecular framework of 2-Phenyl-3H-pyrido[3,4-b][1,4]diazepin-4(5H)-one (C14H11N3O) 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 its high hydrophobicity (logP), 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).

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-Phenyl-3H-pyrido[3,4-b][1,4]diazepin-4(5H)-one 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 FormulaC14H11N3O
Molecular Weight237.26 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963
Nitrogen Atoms3

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