N-(4-chlorophenyl)-1-oxo-2-(pyridin-3-ylmethyl)-1,2-dihydroisoquinoline-4-carboxamide CAS 303995-22-4

Purity 97%+In StockPharmaceutical Standards
CAS No.303995-22-4
Molecular FormulaC22H16ClN3O2
Molecular Weight389.83 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-chlorophenyl)-1-oxo-2-(pyridin-3-ylmethyl)-1,2-dihydroisoquinoline-4-carboxamide CAS 303995-22-4 chemical structure

Description

N-(4-chlorophenyl)-1-oxo-2-(pyridin-3-ylmethyl)-1,2-dihydroisoquinoline-4-carboxamide (CAS 303995-22-4), molecular formula C22H16ClN3O2 and molecular weight 389.83 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, N-(4-chlorophenyl)-1-oxo-2-(pyridin-3-ylmethyl)-1,2-dihydroisoquinoline-4-carboxamide (C22H16ClN3O2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 16.0, corresponding to approximately 16 ring(s) or double-bond equivalent(s). With a molecular weight of 389.83 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

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 FormulaC22H16ClN3O2
Molecular Weight389.83 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms3

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