5471-26-1

Basic information

• Product Name: 4-chloronaphthalene-1-carbaldehyde
• Synonyms: 4-chloronaphthalene-1-carbaldehyde;4-chloro-1-Naphthalenecarboxaldehyde
• CAS NO: 5471-26-1
• Molecular Formula: C₁₁H₇ClO
• Molecular Weight: 190.63
• Mol File: 5471-26-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 333.2°Cat760mmHg
• Flash Point: 159.7°C
• Appearance: /
• Density: 1.295g/cm³
• CAS DataBase Reference: 4-chloronaphthalene-1-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloronaphthalene-1-carbaldehyde(5471-26-1)
• EPA Substance Registry System: 4-chloronaphthalene-1-carbaldehyde(5471-26-1)

Safety Data

• Hazardous Substances Data: 5471-26-1(Hazardous Substances Data)

Upstream product

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

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

Relevant articles and documents

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.

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.