N-(3-Chlorobenzyl)-2-(2,3-dihydro-1H-inden-5-ylcarbonyl)benzenecarboxamide CAS 866133-20-2

Purity 97%+In StockPharmaceutical Standards
CAS No.866133-20-2
Molecular FormulaC24H20ClNO2
Molecular Weight389.87 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Chlorobenzyl)-2-(2,3-dihydro-1H-inden-5-ylcarbonyl)benzenecarboxamide CAS 866133-20-2 chemical structure

Description

CATO manufactures N-(3-Chlorobenzyl)-2-(2,3-dihydro-1H-inden-5-ylcarbonyl)benzenecarboxamide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

N-(3-Chlorobenzyl)-2-(2,3-dihydro-1H-inden-5-ylcarbonyl)benzenecarboxamide (CAS 866133-20-2), molecular formula C24H20ClNO2 and molecular weight 389.87 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, N-(3-Chlorobenzyl)-2-(2,3-dihydro-1H-inden-5-ylcarbonyl)benzenecarboxamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 389.87 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC24H20ClNO2
Molecular Weight389.87 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 chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; 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 Atoms1

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