2412-97-7

Usage

Uses

Used in Organic Synthesis:
3,5-Dichloro-2,4,6-trimethoxypyridine is utilized as a building block in the synthesis of various pharmaceutical and agrochemical products. Its specific properties and reactivity contribute to the development of new materials and substances, enhancing the range of applications in these industries.
Used in Chemical Research and Development:
3,5-Dichloro-2,4,6-trimethoxypyridine serves as a useful tool in chemical research and development due to its unique structural properties. It aids in the exploration of new chemical reactions and the creation of novel compounds, thereby expanding the horizons of organic chemistry.
Used as an Intermediate in Chemical Production:
3,5-Dichloro-2,4,6-trimethoxypyridine is employed as an intermediate in the production of other chemicals. Its role in the synthesis process is crucial for obtaining desired end products, highlighting its importance in the chemical manufacturing industry.

Upstream product

• 91591-88-7 2,4,6-trimethoxypyridine 
• 67-56-1 methanol 
• 2176-62-7 2,3,4,5,6-pentachloropyridine 
• 1737-93-5 3,5-dichloro-2,4,6-trifluoropyridine 
• 16063-69-7 2,4,6-trichloropyridine 
• 2587-02-2 2,6-dichloro-[4]pyridylamine 
• 124-41-4 sodium methylate 

Downstream Products

• 91591-88-7 2,4,6-trimethoxypyridine 

Relevant academic research and scientific papers

Synthesis of new pyridines with oligocations and oxygen nucleophiles.

Nucleophilic substitution of 4-(dimethylamino)pyridine on pentachloropyridine yielded pentakis(pyridine-2,3,4,5,6-pentayl)pyridinium, tris-(3,5-dichloropyridine-2,4,6-triyl)pyridinium, or (tetrachloropyridin-4-yl)pyridinium depending on the reaction conditions. Nucleophilic substitution with water, hydroxides, and alcoholates resulted in new betaines and highly substituted pyridines. [structure: see text]

Polyhalogenated heterocyclic compounds: Part 52. [1] Macrocycles from 3,5-dichloro-2,4,6-trifluoropyridine

Model studies show that displacement of fluorine, rather than chlorine, occurs upon reaction of 3,5-dichloro-2,4,6-trifluoropyridine with sodium methoxide and phenoxide. Subsequent hydro-dechlorination can be achieved by reaction with lithium aluminium hy

Synthesis of alkoxy-substituted pyridines from mono- and tricationic pyridinium salts

Nucleophilic substitution reactions on 4-(4-dimethyl-amino)-pyridinium- substituted tetrachloropyridine with oxygen nucleophiles such as alkoxides and phenolates resulted in the formation of 4- or 2,4-alkoxy- or -phenoxy-substituted chloropyridines depend

Polyfluoroalkoxylation and methoxylation of polychloropyridines

With sodium 2,2,2-trifluoroethoxide, sodium 1,1,1,3,3,3-hexafluoro-2-propoxide and sodium methoxide used as nucleophilic reagents, the alcoholysis reactions of 2,3,4,5,6-pentachloropyridine and 2,3,5,6-tetrachloropyridine were studied. Some new polyfluoroalkoxypyridines have been synthesized. The activities, pathways, mechanism of the alcoholysis reactions are discussed.