128071-79-4

Usage

Uses

Used in Pharmaceutical Industry:
2-Fluoro-4-Bromo-3-Picoline is used as a building block for the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and medications.
Used in Agricultural Products:
2-Fluoro-4-Bromo-3-Picoline is used as a chemical component in the production of agricultural products, potentially enhancing crop protection and yield.
Used in Chemical Research:
2-Fluoro-4-Bromo-3-Picoline is employed as a reagent in chemical research, facilitating the exploration of new chemical reactions and the synthesis of novel compounds.
Used as a Precursor in Chemical Compound Development:
2-Fluoro-4-Bromo-3-Picoline serves as a precursor in the development of new chemical compounds, expanding the scope of chemical applications and innovations.

InChI:InChI=1/C6H5BrFN/c1-4-5(7)2-3-9-6(4)8/h2-3H,1H3

Upstream product

• 372-48-5 2-fluoropyridine 
• 74-88-4 methyl iodide 
• 128071-98-7 4-bromo-2-fluoropyridine 

Downstream Products

• 7631-86-9 SiO₂ 

Relevant academic research and scientific papers

INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE AND METHODS OF THEIR USE

There are disclosed compounds that modulate or inhibit the enzymatic activity of indoleamine 2,3-dioxygenase (IDO), pharmaceutical compositions containing said compounds and methods of treating proliferative disorders, such as cancer, viral infections and/or inflammatory disorders utilizing the compounds of the invention.

TRIAZOLOPYRIDINE COMPOUNDS AND USES THEREOF

A compound of Formula (IA), or a pharmaceutically acceptable salt thereof, is provided that has been shown to be useful for treating a PRC2-mediated disease or disorder: wherein A, R6, R7 and R8 are as defined herein.

Migration du lithium en serie pyridinique: double catalyse et reformage. Acces aux derives de la bromo-2 lithio-3 pyridine et des bromo-4 halogeno-2 lithio-3 pyridines

The lithium of an organolithium-pyridinic derivative can be moved from one position to an another by an intermolecular reaction.Two new reactions are possible for pyridinic organic synthesis: the isomerisation of any lithio derivative to a more stable one, and a reaction that transforms a mixture of various bromo-lithio derivatives into a single one.The processes involved and the experimental tools used are described in terms of the 2-bromo-3-lithio- and 4-bromo-2-halogeno-3-lithiopyridines derivatives synthesis.