2,6-Dimethylpyridine-4-carboxaldehyde, with the CAS number 18206-06-9, is an organic compound belonging to the class of pyridine derivatives. It features a pyridine ring substituted with two methyl groups at the 2 and 6 positions and an aldehyde functional group at the 4 position. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is known for its distinctive aromatic odor, which is characteristic of many pyridine derivatives. The presence of the aldehyde group makes it reactive, particularly in condensation reactions and as a potential precursor in organic synthesis. It is soluble in organic solvents and may exhibit moderate solubility in water. 2,6-Dimethylpyridine-4-carboxaldehyde can be used in various applications, including as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Safety data should be consulted for handling, as it may pose health risks if inhaled or ingested.

2,6-DIMETHYLPYRIDINE-4-CARBOXALDEHYDE

18206-06-9: 2,6-Dimethylisonicotinaldehyde, 2,6-Dimethylpyridine-4-Carbaldehyde

2,6-Dimethylpyridine-4-carbaldehyde

2,6-Dimethylisonicotinaldehyde

4-Pyridinecarboxaldehyde, 2,6-dimethyl-

2,6-Dimethylisonicotinaldehyde is an emission ligand that has a pyridyl structure. It is a heteroleptic compound with a protonated nitrogen atom and a ligand called terpyridine, which is also heteroleptic. The phenyl ring of 2,6-dimethylisonicotinaldehyde is structured and the emission spectra are in the range of green to red. This compound has been used to study the protonation of ligands in solution.

CAS 18206-06-9: 2,6-DIMETHYLPYRIDINE-4-CARBOXALDEHYDE

2,6-Dimethylpyridine-4-carbaldehyde

Ref: FT-D13895

2,6-Dimethylisonicotinaldehyde

Ref: 54-OR946275

2,6-Dimethylisonicotinaldehyde

Ref: 10-F233193

4-Pyridinecarboxaldehyde, 2,6-dimethyl-

Ref: IN-DA0023C0

2,6-Dimethylisonicotinaldehyde

Ref: 3D-TAA20606