15861-51-5

Basic information

• Product Name: (2-bromophenyl)(naphthalen-2-yl)sulfane
• Synonyms: (2-bromophenyl)(naphthalen-2-yl)sulfane
• CAS NO: 15861-51-5
• Molecular Weight: 315.233
• Mol File: 15861-51-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (2-bromophenyl)(naphthalen-2-yl)sulfane(CAS DataBase Reference)
• NIST Chemistry Reference: (2-bromophenyl)(naphthalen-2-yl)sulfane(15861-51-5)
• EPA Substance Registry System: (2-bromophenyl)(naphthalen-2-yl)sulfane(15861-51-5)

Safety Data

• Hazardous Substances Data: 15861-51-5(Hazardous Substances Data)

Upstream product

• 5586-15-2 bis(2-naphthyl)disulfide 
• 244205-40-1 (2-bromophenyl)boronic acid 
• 91-60-1 2-Naphthalenethiol 
• 71112-91-9 bis(2-bromophenyl) disulfide 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 32316-92-0 naphthalene-2-boronic acid 
• 583-55-1 1-Bromo-2-iodobenzene 

Relevant articles and documents

Transition metal complex, polymer, mixture, composition and organic electronic device

The invention discloses a transition metal complex, a polymer, a mixture, a composition and an organic electronic device. When the transition metal complex provided by the invention is used as a light-emitting layer doping material and is applied to an organic electronic device, especially an OLED, the light-emitting efficiency of the device can be improved, and the service life of the device can be prolonged.

Iodine-Promoted Tunable Synthesis of 2-Naphthyl Thioethers and 1-Naphthyl Thioethers

An iodine-promoted regioselective sulfenylation/deoxygenation/aromatization reaction of 1-tetralones with disulfides has been developed. This process could be modified to synthesize 2-naphthyl thioethers and 1-naphthyl thioethers in moderate to excellent

Photostimulated Reactions of o-Dihalobenzenes with Nucleophiles Derived from the 2-Naphthyl System. Competition between Electron Transfer, Fragmentation, and Ring Closure Reactions

The photostimulated reaction of o-dihalobenzenes 2 with 2-naphthoxide ions 1-O gave the substitution product on carbon 1 of the naphthyl moiety with retention of halogen (I, Br, and Cl) 3 as well as the ring closure product benzonaphtholfuran (4), with product 3 being an intermediate in the formation of 4.The products obtained in the photostimulated reaction of 2-naphthalenethiolate ions 1-S with 2 depend on the halogens.When both nucleofugal groups are iodine, only the ring closure product benzonaphthothiophene (10) is obtained.With o-bromoiodobenzene, the photostimulated reaction gave 10 and the substitution product on sulfur with retention of bromine, while with o-chloroiodobenzene the only observed product was the substitution product on sulfur with retention of chlorine.The photostimulated reaction of 2 with 2-naphthaleneselenolate ions 1-Se gave the same amount of cyclized product benzonaphthoselenophene (14) and the substitution product on selenium without retention of halogen 15, although in an overall low yield.It is suggested that all these reactions occur by the SRN1 mechanism.Theoretical studies support the different behavior found with the nucleophiles derived from the 2-naphthyl system.