582-05-8

Basic information

• Product Name: N-(4-fluorophenyl)naphthalen-2-amine
• CAS NO: 582-05-8
• Molecular Formula: C₁₆H₁₂FN
• Molecular Weight: 237.2716
• Mol File: 582-05-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 389°C at 760 mmHg
• Flash Point: 189°C
• Density: 1.224g/cm³
• Vapor Pressure: 2.95E-06mmHg at 25°C
• Refractive Index: 1.682
• CAS DataBase Reference: N-(4-fluorophenyl)naphthalen-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-fluorophenyl)naphthalen-2-amine(582-05-8)
• EPA Substance Registry System: N-(4-fluorophenyl)naphthalen-2-amine(582-05-8)

Safety Data

• Hazardous Substances Data: 582-05-8(Hazardous Substances Data)

Upstream product

• 371-40-4 4-fluoroaniline 
• 135-19-3 β-naphthol 
• 580-13-2 2-bromonaphthalene 
• 93-04-9 2-Methoxynaphthalene 
• 530-93-8 1,2,3,4-tetrahydronaphthalen-2-one 

Downstream Products

• 436-30-6 10-fluoro-12-methyl-benz[a]acridine 
• 385-09-1 10-fluoro-12-phenyl-benz[a]acridine 

Relevant articles and documents

Organic compound and electronic device and device containing the same

The invention relates to the technical field of organic electroluminescent materials, in particular to an organic electroluminescent material 9 with 10 -9 dihydro 9 -10 -dimethyl and oxanthrene and arylamine groups, an electronic device containing the compound and a device. The organic electroluminescent device has lower driving voltage. Higher luminous efficiency and longer service life.

Nucleophilic ipso-Substitution of Aryl Methyl Ethers through Aryl C-OMe Bond Cleavage; Access to Functionalized Bisthiophenes

A metal and solvent free strategy to functionalize aryl methyl ethers through direct nucleophilic substitution of aryl C-OMe bond has been described. A wide range of O, S, N, and C-centered uncharged nucleophiles has been successfully employed. Using this protocol, functional derivatives of bisthiophene have been synthesized in a straightforward way. The reactions are highly atom-efficient and generate methanol as the only byproduct.

B(C6F5)3-catalyzed metal-free hydrogenation of naphthylamines

A catalytic metal-free hydrogenation of naphthylamines using B(C6F5)3 as a catalyst was successfully achieved under mild conditions for the first time to furnish a variety of tetrahydronaphthylamines in 88-99% yields.