1341128-24-2

Basic information

• Product Name: 1,2-bis(4-chlorophenyl)naphthalene
• Synonyms: 1,2-bis(4-chlorophenyl)naphthalene
• CAS NO: 1341128-24-2
• Molecular Weight: 349.259
• Mol File: 1341128-24-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-bis(4-chlorophenyl)naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-bis(4-chlorophenyl)naphthalene(1341128-24-2)
• EPA Substance Registry System: 1,2-bis(4-chlorophenyl)naphthalene(1341128-24-2)

Safety Data

• Hazardous Substances Data: 1341128-24-2(Hazardous Substances Data)

Upstream product

• 1679-18-1 4-Chlorophenylboronic acid 
• 126613-08-9 trifluoromethanesulfonic acid 1-bromonaphthalen-2-yl ester 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 138719-97-8 2-bromonaphthalen-1-yl trifluoromethanesulfonate 
• 771-15-3 2-bromo-1-naphthol 

Relevant articles and documents

ORGANIC ELECTROLUMINESCENCE DEVICE AND DIAMINE COMPOUND FOR ORGANIC ELECTROLUMINESCENCE DEVICE

The invention discloses an organic electroluminescence device and a diamine compound for the organic electroluminescence device. The organic electroluminescence device of an embodiment includes a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer, and a second electrode disposed on the electron transport region, wherein the hole transport region includes a diamine compound represented by Formula 1, thereby showing high emission efficiency:.

Synthesis of 1,2-diarylnaphthalenes by chemoselective Suzuki-Miyaura reactions of 2-bromo-1-(trifluoromethanesulfonyloxy)naphthalene

Suzuki-Miyaura reactions of 2-bromo-1-(trifluoromethanesulfonyloxy) naphthalene, readily available from 1-tetralone in two steps, afforded a variety of 1,2-diarylnaphthalenes. The reactions proceed with excellent chemoselectivity in favor of the bromide position, while the triflate remained unattacked. Georg Thieme Verlag Stuttgart . New York.