2602-36-0

Usage

Uses

Used in Pharmaceutical Industry:
2,6-DIMETHYL-3,5-PYRIDINEDICARBOXYLIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for its ability to form essential structural components of various drug molecules. Its presence in the molecular structure can influence the pharmacological properties, such as solubility, stability, and bioavailability, making it a valuable asset in drug development.
Used in Crop Protection Industry:
In the crop protection industry, 2,6-DIMETHYL-3,5-PYRIDINEDICARBOXYLIC ACID is utilized as a building block in the creation of active ingredients for pesticides and herbicides. Its chemical properties allow for the development of compounds that can effectively control pests and weeds, thereby contributing to improved crop yields and agricultural productivity.
Used in Coordination Chemistry:
2,6-DIMETHYL-3,5-PYRIDINEDICARBOXYLIC ACID is employed as a ligand in coordination chemistry for its ability to form stable complexes with metal ions. This application is significant in various fields, including catalysis, materials science, and the development of new functional materials with tailored properties.
Used in Metal Complexation Reactions:
As a ligand in metal complexation reactions, 2,6-DIMETHYL-3,5-PYRIDINEDICARBOXYLIC ACID plays a crucial role in the formation of metal complexes with specific catalytic, optical, or electronic properties. These complexes find applications in areas such as homogeneous catalysis, sensors, and molecular devices.

InChI:InChI=1/C9H9NO4/c1-4-6(8(11)12)3-7(9(13)14)5(2)10-4/h3H,1-2H3,(H,11,12)(H,13,14)

Upstream product

• 3748-84-3 2,3,5,6-tetramethylpyridine 
• 1149-23-1 diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 1149-24-2 2,6-dimethyl-pyridine-3,5-dicarboxylic acid diethyl ester 

Downstream Products

• 108-48-5 2,6-dimethylpyridine 
• 55275-98-4 2,6-dimethyl-3,5-bis<(phenylamino)carbonyl>pyridine 

Relevant academic research and scientific papers

Study of the acylation reaction of 2,6-dimethyl-3,5-pyridinedicarboxylic acid hydrazides

Acylation of 3-ethoxycarbonyl-2,6-dimethyl-5-pyridinecarboxylic acid hydrazide and 2,6-dimethyl-3,5-pyridinedicarboxylic acid dihydrazide using aromatic acid chlorides gave the corresponding N-aroyl hydrazides. It was found that the hydrazinolysis of 3-ethoxycarbonyl-2,6-dimethyl-5-pyridine-dicarboxylic acid N-aroyl hydrazides occurred not at the ester group but as a rehydrazinolysis reaction at the dihydrazide fragment. 2005 Springer Science+Business Media, Inc.

A peptidomimetic-based thixotropic organogel showing syneresis-induced anti-adhesion against water and ice

The self-assembly, organogelation, syneresis, and anti-adhesion properties of a peptidomimetic containing l-phenylalanine and 2,6-dimethylpyridine 3,5-dicarboxylic acid have been studied in detail. The peptidomimetic forms a transparent gel in aromatic solvents such as benzene, toluene, xylene and chlorobenzene. The hierarchical nature of the self-assembly process in the gel was characterized by a combination of POM and FE-SEM imaging, revealing an entangled fiber network. The rheology measurements then confirmed the formation of a thixotropic organogel. The storage modulus was about one order of magnitude higher than the loss modulus, which indicates the physical crosslinking in the organogel. The gel exhibits significant self-healing properties and allows diffusion of rhodamine 6G through the gel matrix. The peptidomimetic gel shows syneresis under an appropriate environment. The peptidomimetic organogel surfaces exhibit syneresis-induced anti-adhesion properties against ice and water. This peptidomimetic gelator molecule, being economically viable and easy to synthesize, has great prospects in materials chemistry.