4-Chloro-3-[(naphthalen-1-yl)methylidene]-2,3-dihydro-1H-indol-2-one CAS 866137-60-2

Purity 97%+In StockPharmaceutical Standards
CAS No.866137-60-2
Molecular FormulaC19H12ClNO
Molecular Weight305.76 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-3-[(naphthalen-1-yl)methylidene]-2,3-dihydro-1H-indol-2-one CAS 866137-60-2 chemical structure

Description

4-Chloro-3-[(naphthalen-1-yl)methylidene]-2,3-dihydro-1H-indol-2-one (CAS 866137-60-2), molecular formula C19H12ClNO and molecular weight 305.76 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 4-Chloro-3-[(naphthalen-1-yl)methylidene]-2,3-dihydro-1H-indol-2-one (C19H12ClNO) 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. 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.

CATO manufactures 4-Chloro-3-[(naphthalen-1-yl)methylidene]-2,3-dihydro-1H-indol-2-one 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.

Physical & Chemical Properties

Molecular FormulaC19H12ClNO
Molecular Weight305.76 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
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms1

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