18088-10-3

Usage

Uses

Used in Pharmaceutical Industry:
2-Pyridinecarboxylic acid, 4,6-dimethyl-(9CI) is used as a key intermediate in the synthesis of various drugs. Its unique structure allows for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Organic Synthesis:
As a building block for organic synthesis, 2-Pyridinecarboxylic acid, 4,6-dimethyl-(9CI) is utilized in the preparation of a wide range of organic compounds, including dyes, pigments, and other specialty chemicals.
Used in Material Science:
2-Pyridinecarboxylic acid, 4,6-dimethyl-(9CI) has potential applications in the field of material science, where it can be used to develop new materials with specific properties, such as conductivity, magnetism, or catalytic activity.

InChI:InChI=1/C8H9NO2/c1-5-3-6(2)9-7(4-5)8(10)11/h3-4H,1-2H3,(H,10,11)

Upstream product

• 5439-01-0 4,6-dimethylpyridine-2-carbaldehyde 
• 7370-23-2 2,4-dimethyl-6-styryl-pyridine 
• 7584-11-4 4,6-dimethylpyridine-2-carbonitrile 
• 108-47-4 2,4-lutidine 
• 1122-45-8 2,4-dimethylpyridine N-oxide 
• 18087-99-5 4,6-dimethyl-2-(hydroxymethyl)pyridine 
• 13287-63-3 2-(4,6-dimethylpyridin-2-yl)ethanol 
• 108-75-8 2,4,6-trimethyl-pyridine 

Downstream Products

• 69971-38-6 Methyl-4,6-dimethyl-2-pyridincarboxylat 
• 108-47-4 2,4-lutidine 
• 72693-02-8 4,6-dimethylpicolinamide 
• 5407-87-4 2-Amino-4,6-dimethylpyridine 
• 5439-01-0 4,6-dimethylpyridine-2-carbaldehyde 

Relevant academic research and scientific papers

Fe(PyTACN)-catalyzed cis-dihydroxylation of olefins with hydrogen peroxide

A family of iron complexes with general formula [Fe(II)( R,Y,XPyTACN)(CF3SO3)2], where R,Y,XPyTACN=1-[2′-(4-Y-6-X-pyridyl)methyl]-4,7-dialkyl-1,4, 7-triazacyclononane, X and Y refer to the groups at positions 4 and 6 of the pyridine, respectively, and R refers to the alkyl substitution at N-4 and N-7 of the triazacyclononane ring, are shown to be catalysts for efficient and selective alkene oxidation (epoxidation and cis-dihydroxylation) employing hydrogen peroxide as oxidant. Complex [Fe(II)(Me,Me,HPyTACN)(CF 3SO3)2] (7), was identified as the most efficient and selective cis-dihydroxylation catalyst among the family. The high activity of 7 allows the oxidation of alkenes to proceed rapidly (30 min) at room temperature and under conditions where the olefin is not used in large amounts but instead is the limiting reagent. In the presence of 3 mol% of 7, 2 equiv. of H2O2 as oxidant and 15 equiv. of water, in acetonitrile solution, alkenes are cis-dihydroxylated reaching yields that might be interesting for synthetic purposes. Competition experiments show that 7 exhibits preferential selectivity towards the oxidation of cis olefins over the trans analogues, and also affords better yields and high [syn-diol]/[epoxide] ratios when cis olefins are oxidized. For aliphatic substrates, reaction yields attained with the present system compare favourably with state of the art Fe-catalyzed cis-dihydroxylation systems, and it can be regarded as an attractive complement to the iron and manganese systems described recently and which show optimum activity against electron-deficient and aromatic olefins. Copyright

Bioavailable diacylhydrazine ligands for modulating the expression of exogenous genes via an ecdysone receptor complex

The present invention relates to non-steroidal ligands for use in nuclear receptor-based inducible gene expression system, and a method to modulate exogenous gene expression in which an ecdysone receptor complex comprising: a DNA binding domain; a ligand binding domain; a transactivation domain; and a ligand is contacted with a DNA construct comprising: the exogenous gene and a response element; wherein the exogenous gene is under the control of the response element and binding of the DNA binding domain to the response element in the presence of the ligand results in activation or suppression of the gene.