4-([1,2,4]Triazolo[1,5-a]pyridin-6-yl)-5-(6-methyl-pyridin-2-yl)-1H-imidazole-2-carbaldehyde CAS 1352609-91-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1352609-91-6
Molecular FormulaC16H12N6O
Molecular Weight304.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-([1,2,4]Triazolo[1,5-a]pyridin-6-yl)-5-(6-methyl-pyridin-2-yl)-1H-imidazole-2-carbaldehyde CAS 1352609-91-6 chemical structure

Description

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

CATO supplies 4-([1,2,4]Triazolo[1,5-a]pyridin-6-yl)-5-(6-methyl-pyridin-2-yl)-1H-imidazole-2-carbaldehyde (CAS 1352609-91-6), a certified reference material (molecular formula C16H12N6O, MW 304.31 g/mol) for analytical method development and quality control.

Based on its molecular formula C16H12N6O, 4-([1,2,4]Triazolo[1,5-a]pyridin-6-yl)-5-(6-methyl-pyridin-2-yl)-1H-imidazole-2-carbaldehyde contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 304.31 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC16H12N6O
Molecular Weight304.31 g/mol
AppearancePale yellow to yellow crystalline powder
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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms6

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