51417-64-2

Basic information

• Product Name: 2(1H)-Naphthalenone, 1,1-difluoro-
• CAS NO: 51417-64-2
• Molecular Formula: C10H6F2O
• Molecular Weight: 180.154
• Mol File: 51417-64-2.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: 2(1H)-Naphthalenone, 1,1-difluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Naphthalenone, 1,1-difluoro-(51417-64-2)
• EPA Substance Registry System: 2(1H)-Naphthalenone, 1,1-difluoro-(51417-64-2)

Safety Data

• Hazardous Substances Data: 51417-64-2(Hazardous Substances Data)

Upstream product

• 2283-08-1 2-hydroxy-1-naphthalenecarboxylic acid 
• 135-19-3 β-naphthol 
• 91-20-3 naphthalene 
• 140681-68-1 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(trifluoromethanesulfonate) 
• 93-18-5 2-ethoxynaphthalene 
• 93-04-9 2-Methoxynaphthalene 

Downstream Products

• 51417-63-1 1-fluoronaphthalen-2-ol 

Relevant articles and documents

SelectfluorTMon a PolyHIPE Material as Regenerative and Reusable Polymer-Supported Electrophilic Fluorinating Agent

The first recyclable polymer-supported electrophilic fluorinating agent was prepared by reaction of molecular fluorine with the triethylenediamine motif that is grafted onto a poly(4-vinylbenzyl chloride-co-divinylbenzene) polyHIPE material. The resulting

Decarboxylative Fluorination of Arylcarboxylic Acids Promoted by ortho-Hydroxy and Amino Groups

A novel decarboxylative fluorination process has been developed for the synthesis of ortho-hydroxy/amino arylfluorides from salicylic acid analogs, in which the ortho-hydroxy/amino group plays an important role in the transformation. In addition, various arylfluorides are obtained in good to excellent yields under mild conditions.

Fluorination of aromatic compounds with N-fluorobenzenesulfonimide under solvent-free conditions

Reactions of N-fluorobenzenesulfonimide with methylbenzenes, phenols, and phenol ethers were studied under solvent-free conditions. The rate constant ratio for the reactions with mesitylene and durene indicates polar mechanism of the process. Solvent-free fluorination of aromatic compounds with N-fluorobenzenesulfonimide in some cases is more selective than reactions with other N-F reagents in a solvent.