2,6-Dihydroxypyridine is an organic compound characterized by the presence of two hydroxyl (-OH) groups attached to the pyridine ring at the 2 and 6 positions. This compound has a molecular formula of C5H6N2O2 and features a pyridine backbone, which is a six-membered aromatic ring containing one nitrogen atom. The hydroxyl groups contribute to its solubility in water and enhance its reactivity, making it a versatile intermediate in organic synthesis. 2,6-Dihydroxypyridine exhibits properties such as being a weak acid due to the presence of hydroxyl groups, and it can participate in hydrogen bonding, influencing its physical properties and interactions. It is often used in the synthesis of various pharmaceuticals, agrochemicals, and as a ligand in coordination chemistry. Additionally, its derivatives may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken.

2,6-Dihydroxypyridine

626-06-2: 1-Deazauracil, 2(1H)-Pyridinone, 6-hydroxy-, 2(1H)-Pyridone, 6-hydroxy-, 2,6-Dihydroxypyridine, 2-Hydroxy-6-pyridinone, 6-Hydroxy-2(1H)-pyridinone, 6-Hydroxy-2-pyridone

2,6-Dihydroxypyridine is an inhibitor of the enzyme uridine phosphorylase and has been shown to inhibit transcriptional regulation in mammalian cells. It is also a proton source for the synthesis of formyl groups and genotoxic effects. 2,6-Dihydroxypyridine has been shown to be effective as a carbon source for cell growth, but not as an inhibitor of bacterial growth. 2,6-Dihydroxypyridine binds to uridine with high affinity and inhibits the synthesis of uridine monophosphate by competitive inhibition. This leads to inhibition of nucleotide biosynthesis, which can cause inhibition of transcriptional regulation in mammalian cells.

CAS 626-06-2: 2,6-Dihydroxypyridine

2,6-Dihydroxypyridine

Ref: 3D-AAA62606

Pyridine-2,6-diol

Ref: 10-F323520

2,6-Dihydroxypyridine

Ref: 54-OR315026

Pyridine-2,6-diol

Ref: IN-DA003G4U