22282-67-3

Usage

Uses

Used in Pharmaceutical Industry:
4-Iodo-2,6-dimethylpyridine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications, making it a valuable component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4-iodo-2,6-dimethylpyridine serves as a precursor for the production of herbicides and insecticides. Its incorporation into these products contributes to the effectiveness of crop protection agents, enhancing agricultural productivity.
Used as a Reagent in Chemical Reactions:
4-Iodo-2,6-dimethylpyridine is also employed as a reagent in a variety of chemical reactions. Its presence can facilitate or catalyze specific transformations, broadening the scope of achievable organic syntheses.
Used as a Starting Material for Complex Organic Compounds:
Furthermore, 4-iodo-2,6-dimethylpyridine is utilized as a starting material for the synthesis of more complex organic compounds. Its structural features make it a suitable candidate for further functionalization and the construction of intricate molecular architectures.
Due to its diverse applications, 4-iodo-2,6-dimethylpyridine holds significant interest for researchers and professionals in the field of organic chemistry, who continually explore its potential in creating innovative products and processes.

Upstream product

• 3512-80-9 4-amino-2,6-lutidine 
• 325142-95-8 2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine 
• 108-48-5 2,6-dimethylpyridine 
• 13603-44-6 2,6-dimethylpyridin-4-ol 
• 3512-75-2 4-chloro-2,6-lutidine 

Downstream Products

• 84586-42-5 2,6-dimethyl-4(E)-styrylpyridine 
• 3044-71-1 2,6-dimethyl-4-phenylpyridine 
• 103721-78-4 ethyl 2,6-dimethyl-4-pyridineacetate 
• 86520-95-8 4-Ethynyl-2,6-dimethylpyridine 

Relevant academic research and scientific papers

Sterically controlled iodination of arenes via iridium-catalyzed C-H borylation

A mild method to prepare aryl and heteroaryl iodides by sequential C-H borylation and iodination is reported. The regioselectivity of this process is controlled by steric effects on the C-H borylation step and is complementary to existing methods to form aryl iodides. The iodination of boronic esters has potential for the synthesis of radiolabeled aryl iodides, as demonstrated by the concise synthesis of a potential tracer for SPECT imaging.

One-pot iodination of hydroxypyridines

(Chemical Equation Presented) A one-pot, high-yielding iodination of hydroxypyridines and hydroxyquinolines is described. The iodination proceeds under mild conditions, and the products are obtained in high yield without the need for chromatographic purif

Studies on Organometallic Compounds. II. Facile and Convenient Method for the Synthesis of Idoazines through Iododestannation of Trimethylstannylazines

Trimethylsatannyl and bis(trimethylstannyl) derivatives of pyridine, quinoline, and isoquinoline were prepared from the corresponding halo and dihalo (chloro or bromo) derivatives and trimethylstannyl sodium, which was generated in situ from chlorotrimethylsatannane and sodium.These stannyl derivatives readily underwent iododestannation on treatment with iodine to produce the corresponding iodo and diiodo derivatives of pyridine, quinoline, and isoquinoline, respectively, in good yields.Keywords -trimethylsannylazine; bis(trimethylstannyl)azine; iodoazine; diiodoazine; iododestannation; trimethylstannyl sodium; chlorotrimethylstannane