N-(furan-2-ylmethyl)-3-phenyl-1H-indole-2-carboxamide CAS 338401-11-9

Purity 97%+In StockPharmaceutical Standards
CAS No.338401-11-9
Molecular FormulaC20H16N2O2
Molecular Weight316.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(furan-2-ylmethyl)-3-phenyl-1H-indole-2-carboxamide CAS 338401-11-9 chemical structure

Description

Structurally, N-(furan-2-ylmethyl)-3-phenyl-1H-indole-2-carboxamide (C20H16N2O2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 14.0, corresponding to approximately 14 ring(s) or double-bond equivalent(s). With a molecular weight of 316.35 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

N-(furan-2-ylmethyl)-3-phenyl-1H-indole-2-carboxamide (CAS 338401-11-9), molecular formula C20H16N2O2 and molecular weight 316.35 g/mol, is a CATO reference standard with documented purity and traceability.

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.

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 FormulaC20H16N2O2
Molecular Weight316.35 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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms2

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