1-[(4-chlorophenyl)methyl]-N-phenyl-1H-indole-3-carboxamide 10T-1490 860611-50-3 CAS 860611-50-3

Purity 97%+In StockPharmaceutical Standards
CAS No.860611-50-3
Molecular FormulaC22H17ClN2O
Molecular Weight360.84 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-[(4-chlorophenyl)methyl]-N-phenyl-1H-indole-3-carboxamide
10T-1490
860611-50-3 CAS 860611-50-3 chemical structure

Description

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, 1-[(4-chlorophenyl)methyl]-N-phenyl-1H-indole-3-carboxamide 10T-1490 860611-50-3 is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 360.84 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

1-[(4-chlorophenyl)methyl]-N-phenyl-1H-indole-3-carboxamide 10T-1490 860611-50-3 (CAS 860611-50-3), molecular formula C22H17ClN2O and molecular weight 360.84 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 FormulaC22H17ClN2O
Molecular Weight360.84 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms2

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Why CATO?