1285610-45-8

Basic information

• Product Name: 6-chloro-4-(2-chlorophenyl)-2-(p-tolyl)quinoline
• Synonyms: 6-chloro-4-(2-chlorophenyl)-2-(p-tolyl)quinoline
• CAS NO: 1285610-45-8
• Molecular Weight: 364.274
• Mol File: 1285610-45-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-chloro-4-(2-chlorophenyl)-2-(p-tolyl)quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-chloro-4-(2-chlorophenyl)-2-(p-tolyl)quinoline(1285610-45-8)
• EPA Substance Registry System: 6-chloro-4-(2-chlorophenyl)-2-(p-tolyl)quinoline(1285610-45-8)

Safety Data

• Hazardous Substances Data: 1285610-45-8(Hazardous Substances Data)

Upstream product

• 2958-36-3 (2-amino-5-chloro-phenyl)-(2-chloro-phenyl)-methanone 
• 766-97-2 4-n-methylphenylacetylene 
• 784-38-3 2-amino-5-chloro-2'-fluorobenzophenone 
• 122-00-9 para-methylacetophenone 

Relevant articles and documents

Electrophilic Cyclization of 2-Aminophenylprop-1-yn-3-ols into 3-Iodo-6-(aryldiazenyl)quinolines by Using a One-Pot Azo-Coupling and Iodocyclization Sequence

6-(Aryldiazenyl)-3-iodoquinolines were prepared from readily available 2-aminoaryl propargyl alcohols, aryldiazonium salts, and molecular iodine. This three-component one-pot process proceeded through sequential azo-coupling, regioselective iodocyclizatio

Microwave-promoted alkynylation-cyclization of 2-aminoaryl ketones: A green strategy for the synthesis of 2,4-disubstituted quinolines

A series of 2,4-disubstituted quinolines were easily prepared through a one-pot reaction of structurally diverse 2-aminoaryl ketones with various arylacetylenes in the presence of K5CoW12O 403H2O as a reusable a