1312609-72-5

Usage

Structure

Substituted naphthalene derivative
The compound is derived from naphthalene, a fused ring system consisting of two benzene rings, with additional functional groups attached.

Bromine atom position

1
The bromine atom is attached to the first carbon atom of the naphthalene ring.

4-Methoxyphenyl group position

4
The 4-methoxyphenyl group, which consists of a phenyl ring with a methoxy group (-OCH3) attached to the fourth carbon, is attached to the fourth carbon atom of the naphthalene ring.

Use in organic synthesis

Building block for complex molecules
The compound serves as a starting material for the synthesis of more complex organic molecules.

Potential applications

Pharmaceutical and agrochemical industries
Due to its structural properties and reactivity, the compound may be used in the development of new drugs and agrochemicals.

Materials science

Studied for potential use
The compound's properties are being investigated for possible applications in materials science.

Fluorescent probe

Biological studies
The compound has been studied for its potential use as a fluorescent probe in biological research.

Ongoing research and development

Exact uses and properties
Further research is being conducted to determine the specific applications and properties of 1-bromo-4-(4-methoxyphenyl)naphthalene.

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 91-20-3 naphthalene 
• 83-53-4 1,4-dibromonaphthalene 
• 5720-07-0 4-methoxyphenylboronic acid 
• 90-11-9 1-Bromonaphthalene 
• 2298-07-9 4-Bromo-1-naphthylamine 
• 63279-58-3 1-iodo-4-bromo-naphthalene 

Downstream Products

• 1312609-73-6 4-(1-bromonaphthalen-4-yl)phenol 
• 1312609-74-7 C₂₂H₂₃BO₃ 
• 1312609-75-8 C₂₈H₂₉N₃O₃ 
• 1312609-76-9 C₂₉H₂₈F₃N₃O₅S 
• 1312609-77-0 C₃₄H₄₀BN₃O₄ 
• 1312609-78-1 C₄₃H₄₄N₆O₄ 
• 1312608-67-5 C₃₅H₃₈N₆O₂ 
• 1312608-66-4 C₄₂H₄₉N₇O₅ 
• 1312609-79-2 C₃₇H₄₁N₇O₃ 
• 1312608-53-9 C₄₅H₄₇N₇O₄ 
• 1312609-80-5 C₄₃H₄₄N₆O₃ 
• 1312609-81-6 C₃₈H₃₆N₆O 
• 1312608-54-0 C₄₅H₄₇N₇O₄ 
• 1351953-37-1 4-(4-(4-(2-ethylhexyloxy)phenyl)naphthalen-1-yl)benzonitrile 

Relevant academic research and scientific papers

WAVELENGTH CONVERSION MATERIAL FOR HIGHLY EFFICIENT DYE-SENSITIZED SOLAR CELL, AND PREPARATION METHOD THEREOF

Novel compounds represented by the present invention refers to formula 1 or formula 2, said novel compounds including wavelength change material, and including said wavelength change material relates to dye-sensitized solar cell.

Wavelength conversion lanthanide(III)-cored complex for highly efficient dye-sensitized solar cells

Lanthanide(III)-cored complex as a wavelength conversion material has been successfully designed and synthesized for highly efficient dye-sensitized solar cells, for the first time, since light with a short wavelength has not been effectively used for generating electric power owing to the limited absorption of these DSSCs in the UV region. A black dye (BD) was chosen and used as a sensitizer, because BD has a relatively weak light absorption at shorter wavelengths. The overall conversion efficiency of the BD/WCM device was remarkably increased, even with the relatively small amount of WCM added to the device. The enhancement in Voc by WCM, like DCA, could be correlated with the suppression of electron recombination between the injected electrons and I3 - ions. Furthermore, the short-circuit current density was significantly increased by WCM with a strong UV light-harvesting effect. The energy transfer from the Eu(III)-cored complex to the TiO2 film occurred via the dye, so the number of electrons injected into the TiO2 surface increased, i.e., the short-circuit current density was increased. As a result, BD/WCM-sensitized solar cells exhibit superior device performance with the enhanced conversion efficiency by a factor of 1.22 under AM 1.5 sunlight: The photovoltaic performance of the BD/WCM-based DSSC exhibited remarkably high values, Jsc of 17.72 mA/cm2, Voc of 720 mV, and a conversion efficiency of 9.28% at 100 mW cm-2, compared to a standard DSSC with Jsc of 15.53 mA/cm2, Voc of 689 mV, and a conversion efficiency of 7.58% at 100 mW cm-2. Therefore, the Eu(III)-cored complex is a promising candidate as a new wavelength conversion coadsorbent for highly efficient dyesensitized solar cells to improve UV light harvesting through energy transfer processes. The abstract should be a single paragraph which summaries the content of the article.

NOVEL INHIBITORS OF HEPATITIS C VIRUS REPLICATION

The embodiments provide compounds of the general Formulae I, II, III, IV, or V as well as compositions, including pharmaceutical compositions, comprising a subject compound. The embodiments further provide treatment methods, including methods of treating a hepatitis C virus infection and methods of treating liver fibrosis, the methods generally involving administering to an individual in need thereof an effective amount of a subject compound or composition.