93989-32-3

Basic information

• Product Name: 2-BROMO-1-PHENYL-NAPHTHALENE
• Synonyms: 2-BROMO-1-PHENYL-NAPHTHALENE
• CAS NO: 93989-32-3
• Molecular Formula: C₁₆H₁₁Br
• Molecular Weight: 283.16254
• Mol File: 93989-32-3.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-BROMO-1-PHENYL-NAPHTHALENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-1-PHENYL-NAPHTHALENE(93989-32-3)
• EPA Substance Registry System: 2-BROMO-1-PHENYL-NAPHTHALENE(93989-32-3)

Safety Data

• Hazardous Substances Data: 93989-32-3(Hazardous Substances Data)

Usage

General Description

2-Bromo-1-phenyl-naphthalene is a chemical compound with the formula C16H11Br. It is a brominated derivative of naphthalene with a phenyl group attached. 2-BROMO-1-PHENYL-NAPHTHALENE is used in organic synthesis and as a building block in the production of pharmaceuticals and agrochemicals. It is also used as a reagent in chemical reactions to introduce the bromine atom into organic molecules. 2-Bromo-1-phenyl-naphthalene is a solid at room temperature and is insoluble in water but soluble in organic solvents. It is considered to be a hazardous compound and should be handled with care, following proper safety precautions.

Upstream product

• 1961-97-3 3-phenyl-1H-indene 
• 101278-61-9 1-Phenyl-2-brom-3,4-dihydro-naphthalin 
• 62969-97-5 1,4-diphenyl-3-butyn-2-ol 
• 83-33-0 inden-1-one 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 122-78-1 phenylacetaldehyde 
• 932-87-6 1-Bromo-2-phenylacetylene 
• 5438-13-1 1,2-dibromonaphthalene 
• 98-80-6 phenylboronic acid 
• 96-09-3 styrene oxide 

Downstream Products

• 100736-53-6 Bis-<1-phenyl-naphthyl-(2)>-chlorarsin 
• 206-44-0 fluoranthene 
• 107928-58-5 bis-(1-phenyl-naphthalen-2-yl)-arsinic acid 

Relevant articles and documents

MeOTf-catalyzed formal [4?+?2] annulations of styrene oxides with alkynes leading to polysubstituted naphthalenes through sequential electrophilic cyclization/ring expansion

MeOTf-catalyzed formal [4 + 2] annulation of styrene oxides with alkynes to afford polysubstituted naphthalenes has been realized, which undergoes sequential electrophilic cyclization/ring expansion. A range of substrates were tolerated in the formation of naphthalene derivatives with high regioselectivity in satisfactory yields. The reaction could also be carried out on gram scale.

Nitrogen-containing compounds Organic electroluminescent device and electronic device using the same

The present application provides a nitrogen containing compound, an organic electroluminescent device using same, and an electronic device. A chemical structure of an organic compound in the present invention comprises a carbazole ring. The organic compound can be used as the material of a light-emitting layer in an electroluminescent device to improve the efficiency of the organic electroluminescent device and prolong the service life thereof.

Gold-Catalyzed Electrophilic Addition to Arylalkynes. A Facile Method for the Regioselective Synthesis of Substituted Naphthalenes

An interesting gold-catalyzed electrophilic addition to arylalkyne to synthesize substituted naphthalenes has been presented. Different metal hexafluoroantimonates have also been found to effect the transformation. Counter anion and oxo- and alkynophilicities of catalytic gold species might play an important role in this annulation reaction.