22082-93-5

Basic information

• Product Name: Naphthalene, 1-broMo-2-phenyl-
• Synonyms: Naphthalene, 1-broMo-2-phenyl-;1-Bromo-2-phenylnaphthalene
• CAS NO: 22082-93-5
• Molecular Formula: C₁₆H₁₁Br
• Molecular Weight: 283.16254
• Mol File: 22082-93-5.mol
• Article Data: 11

Chemical Properties

• Melting Point: 63.0 to 67.0 °C
• Boiling Point: 170°C/0.2mmHg(lit.)
• Appearance: /
• CAS DataBase Reference: Naphthalene, 1-broMo-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Naphthalene, 1-broMo-2-phenyl-(22082-93-5)
• EPA Substance Registry System: Naphthalene, 1-broMo-2-phenyl-(22082-93-5)

Safety Data

• Hazardous Substances Data: 22082-93-5(Hazardous Substances Data)

Usage

General Description

1-Bromo-2-phenyl-naphthalene is a chemical compound with the molecular formula C17H11Br. It is also known by its systematic name, 2-Bromophenyl Naphthalene. Naphthalene, 1-bromo-2-phenyl- is recognized by its chemical abstracts service (CAS) number 171596-05-1. As an organic substance, it belongs to the class of compounds known as aryloxy compounds, which are aromatic compounds containing an oxygen atom directly bonded to an aryl group. This substance is relatively unexplored as there is limited data available regarding its properties and interactions. Therefore, its potential uses, hazards or benefits still remain largely unknown.

Upstream product

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Downstream Products

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• 1394846-67-3 1-(4-methoxylphenyl)-2-phenylnaphthalene 
• 612086-26-7 (+/-)-3-bromo-4-chloro-5-(2-phenylnaphthalen-1-yl)pyridine 
• 612086-27-8 4-chloro-3-(2-phenyl-naphthalen-1-yl)pyridine 
• 278600-44-5 (+/-)-diethyl-[3-(2-phenylnaphthalen-1-yl)pyridin-4-yl]amine 
• 69452-56-8 1-iodo-2-phenylnaphthalene 

Relevant articles and documents

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.

Dichloroimidazolidinedione-activated one-pot Suzuki–Miyaura cross-coupling of phenols

The first general method for the Suzuki-type cross-coupling of phenols with aryl boronic acids using dichloroimidazolidinedione (DCID) as a new reagent is presented. In the presence of DCID and Pd/metal–organic framework (MOF), coupling of aryl boronic acids with a wide range of phenols, was carried out smoothly in tetrahydrofuran (THF) at reflux conditions to afford the cross-coupling products in good to excellent yields. The structures of all compounds were corroborated by 1H- and 13C-NMR. A plausible mechanism for this type of reaction is proposed.

NOVEL ORGANIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

The present invention provides a novel stable benzo[a]naphtho[2,1-c]tetracene compound and an organic light-emitting device including the compound. Provided is an organic compound represented by Formula [1] described in Claim 1. In Formula [1], R1 to R16 each independently selected from a hydrogen atom, a halogen atom, an alkyl group having 1 to 4 carbon atoms, a cyano group, a diphenylamino group, a pyridyl group, and an aryl group.