1393817-78-1

Basic information

• Product Name: 8-(4-broMophenyl)quinoline
• Synonyms: 8-BPQ
• CAS NO: 1393817-78-1
• Molecular Formula: C15H10BrN
• Molecular Weight: 284.1506
• Mol File: 1393817-78-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 391.4±22.0 °C(Predicted)
• Appearance: /
• Density: 1.433±0.06 g/cm3(Predicted)
• PKA: 4.13±0.17(Predicted)
• CAS DataBase Reference: 8-(4-broMophenyl)quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 8-(4-broMophenyl)quinoline(1393817-78-1)
• EPA Substance Registry System: 8-(4-broMophenyl)quinoline(1393817-78-1)

Safety Data

• Hazardous Substances Data: 1393817-78-1(Hazardous Substances Data)

Usage

General Description

8-(4-bromophenyl)quinoline is a chemical compound with the molecular formula C15H10BrN and a molecular weight of 283.15 g/mol. It is a quinoline derivative with a 4-bromophenyl group attached at the 8th position of the quinoline ring. 8-(4-broMophenyl)quinoline can be used in various applications such as organic synthesis, pharmaceuticals, and material science. It may have potential bioactive properties due to its structural features, making it of interest for drug discovery and development. Additionally, it may also have potential uses in the development of organic electronic devices and luminescent materials. However, as with any chemical compound, it is important to handle and use 8-(4-bromophenyl)quinoline with proper safety precautions due to its potential hazards.

Upstream product

• 86-58-8 8-quinolinylboronic acid 
• 589-87-7 1,4-bromoiodobenzene 
• 1613-37-2 Quinoline N-oxide 
• 10602-01-4 p-bromobenzaldehyde 1,3-dioxolane 
• 91-22-5 quinoline 
• 5467-74-3 4-Bromophenylboronic acid 

Downstream Products

• 123172-87-2 8-(phenylethynyl)quinoline 

Relevant articles and documents

Rh(III)-Catalyzed N-Nitroso Directed C-H Arylation for Facile Construction of Diverse N-Hetero Biaryl Compounds

A Rh(III)-catalyzed C?H arylation reaction of N-nitrosoanilines has been developed in which arylboronic acids were used as arylation reagents. It provides an efficient strategy for the synthesis of N-nitroso-[1,1′-biphenyl]-2-amine, which is an important starting material for the synthesis of N-hetero biaryl compounds, such as 2-amine-1,1′-biphenyl, carbazole, phenanthridone. This protocol can be applied to various N-alkyl substituted N-nitrosoanilines and N-nitrosoanilines with substituents on the phenyl ring. Arylboronic acids with both electron-donating and electron-withdrawing groups are tolerated.

Ru-Catalyzed Deoxygenative Regioselective C8-H Arylation of Quinoline N-Oxides

Regioselective C-H functionalization on quinolines is of high interest to lead to value-added products. Herein, we describe the development of Ru-catalyzed deoxygenative regioselective C8 arylation of quinoline N-oxides with arylboronic esters. Mechanistic studies revealed that it proceeds in a tandem process of arylation and then deoxygenation, wherein both steps were found to be catalytic with the ruthenium species.