(S)-2-(4-((4-Oxobenzo[d][1,2,3]triazin-3(4H)-yl)methyl)cyclohexane-1-carboxamido)-2-phenylacetic acid CAS 1217458-07-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1217458-07-5
Molecular FormulaC23H24N4O4
Molecular Weight420.46 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-(4-((4-Oxobenzo[d][1,2,3]triazin-3(4H)-yl)methyl)cyclohexane-1-carboxamido)-2-phenylacetic acid CAS 1217458-07-5 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

(S)-2-(4-((4-Oxobenzo[d][1,2,3]triazin-3(4H)-yl)methyl)cyclohexane-1-carboxamido)-2-phenylacetic acid (CAS 1217458-07-5), molecular formula C23H24N4O4 and molecular weight 420.46 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a flavonoid core, an amide group, a hydroxyl group, an ether linkage, (S)-2-(4-((4-Oxobenzo[d][1,2,3]triazin-3(4H)-yl)methyl)cyclohexane-1-carboxamido)-2-phenylacetic acid is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 420.46 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

Physical & Chemical Properties

Molecular FormulaC23H24N4O4
Molecular Weight420.46 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°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.)1990
Nitrogen Atoms4

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