5471-26-1

Upstream product

• 1013-04-3 4-chloro-1-naphthoic acid 
• 4885-02-3 Dichloromethyl methyl ether 
• 90-13-1 1-Chloronaphthalene 
• 17075-39-7 4-chloro-1-methyl-naphthalene 

Downstream Products

• 146517-62-6 (E)-3-(4-Chloro-naphthalen-1-yl)-1-(2-hydroxy-5-methyl-phenyl)-propenone 
• 146517-63-7 (E)-1-(5-Chloro-2-hydroxy-phenyl)-3-(4-chloro-naphthalen-1-yl)-propenone 
• 146517-66-0 (E)-3-(4-Chloro-naphthalen-1-yl)-1-(3,5-dichloro-2-hydroxy-phenyl)-propenone 
• 109297-22-5 4--1-naphthonitrile 
• 136613-48-4 4-chloro-2-naphthonitrile 
• 72606-55-4 [Methyl-(1-methyl-2-phenyl-ethyl)-amino]-acetic acid [1-(4-chloro-naphthalen-1-yl)-meth-(E)-ylidene]-hydrazide 
• 72606-53-2 Phenethylamino-acetic acid [1-(4-chloro-naphthalen-1-yl)-meth-(E)-ylidene]-hydrazide 
• 146517-61-5 (E)-3-(4-Chloro-naphthalen-1-yl)-1-(2-hydroxy-phenyl)-propenone 
• 146517-67-1 (E)-3-(4-Chloro-naphthalen-1-yl)-1-(2-hydroxy-3,5-diiodo-phenyl)-propenone 
• 146517-64-8 (E)-1-(5-Bromo-2-hydroxy-phenyl)-3-(4-chloro-naphthalen-1-yl)-propenone 
• 146517-65-9 (E)-1-(5-Chloro-2-hydroxy-4-methyl-phenyl)-3-(4-chloro-naphthalen-1-yl)-propenone 

Relevant academic research and scientific papers

Palladium-Catalyzed Regiospecific peri- And ortho-C-H Oxygenations of Polyaromatic Rings Mediated by Tunable Directing Groups

An efficient divergent approach of Pd-catalyzed C-H oxygenation of polyaromatic rings is described. Reversible directing groups enable regiospecific peri- and ortho-oxygenation to readily access a wide array of polyaromatic phenols without pre- and postmanipulation of directing groups. The systematic mechanistic investigation, including deuterium-labeling experiments, palladacycle trapping, and DFT calculations, reveals that the tunable ligand-assisted C-H bond cleavage played a crucial role during the reaction process.

USE OF DISUBSTITUTED BENZENES TO CONTROL INSECTICIDE-RESISTANT PESTS

The invention is in the technical field of insect control and relates to the use of a disubstituted benzenes for controlling insecticide-resistant pests such as mosquitoes and cockroaches.

HETEROCYCLIC COMPOUNDS, METHODS OF MAKING THEM AND THEIR USE IN THERAPY

In part, the present invention is directed to antibacterial compounds of formula (I) wherein A is a bicyclic heteroaryl ring or a tricyclic ring and R2 is an heterocyclic residue; L is a bond, or L is alkyl, alkenyl or cycloalkyl.

Reactions of Organic Anions. Part 180. Orientation of the Carbanion Attack of Chloromethyl p-Tolyl Sulphone on 1-Cyanonaphthalene Derivatives

The carbanion of chloromethyl p-tolyl sulphone reacts with cyanonaphthalene derivatives to give bis-annulated products and/or SNAr products and/or products of nucleophilic substitution of hydrogen depending on the structure of the substrates and on reaction conditions.The orientation of the initial carbanion attack is discussed.