1-[(4-chlorophenyl)methyl]-N-(4-methoxyphenyl)-1H-indole-3-carboxamide 10T-1488 860611-49-0 CAS 860611-49-0

Purity 97%+In StockPharmaceutical Standards
CAS No.860611-49-0
Molecular FormulaC23H19ClN2O2
Molecular Weight390.86 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-[(4-chlorophenyl)methyl]-N-(4-methoxyphenyl)-1H-indole-3-carboxamide
10T-1488
860611-49-0 CAS 860611-49-0 chemical structure

Description

As a certified reference material (CRM), 1-[(4-chlorophenyl)methyl]-N-(4-methoxyphenyl)-1H-indole-3-carboxamide 10T-1488 860611-49-0 meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

CATO supplies 1-[(4-chlorophenyl)methyl]-N-(4-methoxyphenyl)-1H-indole-3-carboxamide 10T-1488 860611-49-0 (CAS 860611-49-0), a certified reference material (molecular formula C23H19ClN2O2, MW 390.86 g/mol) for analytical method development and quality control.

The molecular framework of 1-[(4-chlorophenyl)methyl]-N-(4-methoxyphenyl)-1H-indole-3-carboxamide 10T-1488 860611-49-0 (C23H19ClN2O2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

Physical & Chemical Properties

Molecular FormulaC23H19ClN2O2
Molecular Weight390.86 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)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms2

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