38749-93-8

Usage

Uses

Used in Organic Synthesis:
3,6-Dibromo-2,5-lutidine is used as a building block or intermediate in the field of organic synthesis, enabling the creation of more complex chemical compounds.
Used in Halogenation Reactions:
Due to the presence of bromine atoms, 3,6-Dibromo-2,5-lutidine is utilized in various halogenation reactions, contributing to the synthesis of a wide range of chemical products.
For detailed information regarding the physical and chemical properties, safety precautions, and handling procedures of 3,6-Dibromo-2,5-lutidine, it is recommended to refer to its Material Safety Data Sheet (MSDS).

InChI:InChI=1/C7H7Br2N/c1-4-3-6(8)5(2)10-7(4)9/h3H,1-2H3

Upstream product

• 589-93-5 2,5-dimethylpyridine 

Downstream Products

• 53428-02-7 3,6-dimethyl-2-pyridone 

Relevant academic research and scientific papers

Synthesis of highly functionalized pyridines for planar polymers. Maximized π-conjugation in electron deficient macromolecules

Synthetic routes to planar polypyridines are described. Two pyridine monomers for the step growth polymerization are prepared starting from 2,5- 1utidine via 2,5-dibromopyridine-3,6-dicarboxylic acid as the common intermediate, The dicarboxylic acid serve

Controlled oxygen release from pyridone endoperoxides promotes cell survival under anoxic conditions

In tissue engineering, survival of larger constructs remains challenging due to limited supply of oxygen caused by a lack of early vascularization. Controlled release of oxygen from small organic molecules represents a possible strategy to prevent cell death under anoxic conditions. A comprehensive study of methylated pyridone-derived endoperoxides has led to the development of water-soluble molecules that undergo retro-Diels-Alder reactions in aqueous environment releasing oxygen in high yield and with half-lives of up to 13 h. These molecules in combination with vitamin C as singlet oxygen quencher significantly improved survival of 3T3 fibroblasts and rat smooth muscle cells challenged with oxygen-depleted conditions.