22082-93-5

Usage

Uses

Due to the limited data available on Naphthalene, 1-bromo-2-phenyl-, its applications are not well-defined. However, based on its classification as an aryloxy compound, it can be inferred that it may have potential uses in various industries, such as:
Used in Chemical Synthesis Industry:
Naphthalene, 1-bromo-2-phenyl-, could be used as an intermediate or a building block in the synthesis of more complex organic compounds, given its aromatic nature and the presence of a bromine atom that can be a reactive site for further chemical reactions.
Used in Pharmaceutical Industry:
As an aryloxy compound, Naphthalene, 1-bromo-2-phenyl-, might have potential applications in the development of new pharmaceuticals, particularly in the area of drug discovery and design, where its unique structure could be exploited to create novel therapeutic agents.
Used in Material Science:
Naphthalene, 1-bromo-2-phenyl-'s aromatic structure and bromine atom could make it a candidate for use in the development of new materials with specific properties, such as in the field of organic electronics or as a component in advanced composite materials.

Upstream product

• 126613-08-9 trifluoromethanesulfonic acid 1-bromonaphthalen-2-yl ester 
• 100-58-3 phenylmagnesium bromide 
• 69-96-5 Phenylserin 
• 581-97-5 2-acetylaminonaphthalene 
• 59046-72-9 o-(phenylethynyl)benzaldehyde 
• 536-74-3 phenylacetylene 
• 573-97-7 1-bromo-2-naphthol 
• 98-80-6 phenylboronic acid 
• 108-86-1 bromobenzene 
• 42768-98-9 1-bromo-2-naphthyl p-toluenesulfonate 
• 855879-70-8 N-[2]naphthyl-N-nitroso-acetamide 
• 612-94-2 2-phenylnaphthalene 

Downstream Products

• 612086-25-6 4,4,5,5-tetramethyl-2-(2-phenyl-naphthalen-1-yl)-[1,3,2]dioxaborolane 
• 1439303-40-8 C₄₂H₂₇Cl 
• 1341128-33-3 2-(phenyl)-1-(2-methoxyphenyl)naphthalene 
• 1416339-69-9 1-(4-methylphenyl)-2-phenylnaphthalene 
• 1394846-67-3 1-(4-methoxylphenyl)-2-phenylnaphthalene 

Relevant academic research and scientific papers

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.

Selective synthesis of 1-halonaphthalenes by copper-catalyzed benzannulation

The synthesis of 1-halonaphthalenes by the Cu-catalyzed benzannulation reaction of 2-(phenylethynyl)benzaldehyde and alkynes in the presence of the halogen reagents such as NBS, NCS, and NIS, was developed. This protocol afforded various type of 1-halonap

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.

Material for organic device and organic electroluminescent device using same (by machine translation)

The compound according to claim 1, which is represented by the following general formula. When a polycyclic aromatic compound having a bulky substituent in a molecule is used as a material for an organic device, an organic EL device having good quantum efficiency can be provided, for example. In particular, since the use concentration can be relatively high, concentration quenching can be suppressed, which is advantageous in the device manufacturing process. (In General Formula (1), R represents a hydrogen atom or a methyl group. 1 R/R3 R/R4 ～ R7 R/R8 ～ R11 R/R12 ～ R15 Is independently hydrogen, aryl, or the X, and X is each independently hydrogen, aryl, or the like. 1 Silver - O or — AOMARKENCODEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGXDEGX1 Z2 At least 1 hydrogen in the compound of general formula (1) may be substituted with halogen or deuterium. (by machine translation)

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.

Rhenium-catalyzed regioselective synthesis of 1,2-disubstituted naphthalenes

Rhenium-catalyzed coupling reaction of alkynes with phenylacetaldehyde dimethylacetal in the presence of H2O regioselectively afforded the corresponding 1,2-disubstituted naphthalenes.

Azaboradibenzo[6]helicene: Carrier inversion induced by helical homochirality

Azaboradibenzo[6]helicene, a new semiconductor material possessing helical chirality, has been synthesized via a tandem bora-Friedel-Crafts-type reaction. Unprecedented carrier inversion between the racemate (displaying p-type semiconductivity) and the si

CuX2-mediated [4+2] benzannulation as a new synthetic tool for stereoselective construction of haloaromatic compounds

The CuX2-mediated reaction of enynal units, including ortho-alkynylbenzaldehydes, with alkynes gives a variety of haloaromatic compounds stereoselectively in good to high yields. 2,2′-Binaphthyl skeletons are also readily prepared by the reacti

PROCESS FOR THE PREPARATION OF ATROPISOMERIC ANALOGUES OF 4-AMINOPYRIDINE

The present invention relates to a process for the preparation of 3,4-disubstituted pyridines from commercially available starting materials. In particular, the invention relates to the process for the preparation for a compound of formula (I) wherein a c

Concise synthesis, preparative resolution, absolute configuration determination, and applications of an atropisomeric biaryl catalyst for asymmetric acylation

A new three-step synthesis and resolution of nucleophilic catalyst 1 suitable for large-scale preparation has been developed, and this catalyst has been shown to be effective for the kinetic resolution and asymmetric desymmetrization of a range of sec-alcohol substrates.