777940-46-2

Usage

Chemical structure

A pyridinone ring with a methyl group at the 6th position and an iodine atom at the 3rd position.

Type of compound

A derivative of pyridinone.

Applications

Pharmaceutical and organic synthesis.

Use

As a building block for the synthesis of complex organic compounds and as a precursor for the production of other chemicals with specific properties.

Iodine substituent

Makes it useful for certain types of chemical reactions and as a reagent in organic synthesis.

Upstream product

• 3279-76-3 6-hydroxy-2-methylpyridine 
• 3279-76-3 6-methyl-2(1H)-pyridone 

Downstream Products

• 927869-51-0 3-(4-ethyl-phenylsulfanyl)-6-methyl-pyridin-2-ol 
• 777940-48-4 2-Chloro-3-(4-methoxyphenylsulfanyl)-6-methylpyridine 
• 777940-32-6 3-[6-Methyl-2-(2,4,6-trimethylphenylamino)-pyridine-3-sulfonyl]-phenol 
• 777939-85-2 4-[6-Methyl-2-(2,4,6-trimethylphenylamino)-pyridine-3-sulfonyl]-phenol 
• 777940-31-5 [3-(3-Methoxybenzenesulfonyl)-6-methylpyridin-2-yl]-(2,4,6-trimethylphenyl)-amine 
• 777939-84-1 [3-(4-Methoxybenzenesulfonyl)-6-methylpyridin-2-yl]-(2,4,6-trimethylphenyl)-amine 
• 927870-65-3 2-chloro-3-(4-ethyl-benzenesulfonyl)-6-methyl-pyridine 
• 878140-78-4 2-chloro-6-methyl-3-(toluene-4-sulfonyl)-pyridine 

Relevant academic research and scientific papers

Synthesis and evaluation of 2-anilino-3-phenylsulfonyl-6-methylpyridines as corticotropin-releasing factor1 receptor ligands

A novel series of 2-anilino-3-phenylsulfonyl-6-methylpyridines was synthesized and evaluated as corticotropin-releasing factor receptor ligands. Structure-activity relationship studies focused primarily on optimization of the 3-phenylsulfonyl group. Compo

Pyridinyl derivatives for the treatment of depression

The present invention relates to novel heterocyclic antagonists of Formula (I) and pharmaceutical compositions comprising said antagonists of the corticotropin releasing factor receptor (“CRF receptor”) useful for the treatment of depression, anxiety, aff