168823-65-2

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
2-(3-BROMO-4-METHOXYPHENYL)PYRIDINE is used as a synthetic intermediate for the production of various pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a wide range of compounds with potential therapeutic and pesticidal properties.
Used in Organic Electronics:
In the field of organic electronics, 2-(3-BROMO-4-METHOXYPHENYL)PYRIDINE is utilized in the development of organic light-emitting diodes (OLEDs) and other organic electronic materials. Its electron-withdrawing and donating properties make it a promising candidate for enhancing the performance of these devices.
Safety Considerations:
It is crucial to handle 2-(3-BROMO-4-METHOXYPHENYL)PYRIDINE with care due to its potential hazardous effects on health and the environment. Proper safety measures should be implemented during its synthesis, storage, and application to minimize risks.

InChI:InChI=1/C12H10BrNO/c1-15-12-6-5-9(8-10(12)13)11-4-2-3-7-14-11/h2-8H,1H3

Upstream product

• 5957-90-4 4-(2-pyridinyl)anisole 
• 109-04-6 2-bromo-pyridine 
• 5720-07-0 4-methoxyphenylboronic acid 

Downstream Products

• 1565863-97-9 C₁₂H₈Br₃NO 
• 1313359-14-6 2-(2,5-dibromo-4-methoxyphenyl)pyridine 
• 1313359-15-7 2-(2,3-dibromo-4-methoxyphenyl)pyridine 

Relevant academic research and scientific papers

2 - (3 - halogen-phenyl) pyridine derivatives for preparing method

The invention discloses a preparation method of a 2-(3-halogen phenyl) pyridine derivative. The preparation method comprises the following steps: dissolving 2-phenylpyridine or substitutive 2-phenylpyridine (I) and N-halogenated butyl diimide (II) into a

Directed meta-Selective Bromination of Arenes with Ruthenium Catalysts

A Ru-catalyzed direct C?H activation/meta-bromination of arenes bearing pyridyl, pyrimidyl, and pyrazolyl directing groups has been developed. A series of bromo aryl pyridines and pyrimidines have been synthesized, and further coupling reactions have also been demonstrated for a number of representative functionalized arenes. Preliminary mechanistic studies have revealed that this reaction may proceed through radical-mediated bromination when NBS is utilized as the bromine source. This type of transformation has opened up a new direction for the radical non-ipso functionalization of metal with regard to future C?H activation development that would allow the remote functionalization of aromatic systems.

Copper-catalyzed aromatic C-H bond halogenation using lithium halides as halogenating reagents

The copper-catalyzed C-H halogenation of 2-aryl-pyridines containing a variety of electron-withdrawing and electron-donating substituents was described. It is worth noting that cheap and easy-to-handle lithium halides were utilized as the halogen sources. Georg Thieme Verlag Stuttgart · New York.