6-Ethyl-2-(4-isopropoxyphenyl)quinoline-4-carbonyl chloride CAS 1160261-06-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1160261-06-2
Molecular FormulaC21H20ClNO2
Molecular Weight353.84 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Ethyl-2-(4-isopropoxyphenyl)quinoline-4-carbonyl chloride CAS 1160261-06-2 chemical structure

Description

CATO manufactures 6-Ethyl-2-(4-isopropoxyphenyl)quinoline-4-carbonyl chloride 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.

CATO supplies 6-Ethyl-2-(4-isopropoxyphenyl)quinoline-4-carbonyl chloride (CAS 1160261-06-2), a certified reference material (molecular formula C21H20ClNO2, MW 353.84 g/mol) for analytical method development and quality control.

Based on its molecular formula C21H20ClNO2, 6-Ethyl-2-(4-isopropoxyphenyl)quinoline-4-carbonyl chloride contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 353.84 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 FormulaC21H20ClNO2
Molecular Weight353.84 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 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Nitrogen Atoms1

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