3,6-Diiodopyridazine is a chemical compound characterized by its pyridazine ring, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 3 and 6, substituted with iodine atoms. This compound typically exhibits a pale yellow to brownish appearance and is known for its potential applications in various fields, including pharmaceuticals and agrochemicals. The presence of iodine atoms enhances its reactivity and can influence its biological activity, making it a subject of interest in medicinal chemistry. 3,6-Diiodopyridazine is generally soluble in organic solvents, and its properties can be affected by the presence of functional groups or other substituents. The compound's molecular structure allows for various chemical reactions, including electrophilic substitutions and coupling reactions, which can be utilized in synthetic organic chemistry. Safety data should be consulted, as halogenated compounds can pose health risks, and appropriate handling procedures should be followed.

3,6-Diiodopyridazine

20698-04-8: Pyridazine, 3,6-Diiodo-, 3,6-Diidopyridazine, 3,6-Diiodopyridazine

Pyridazine, 3,6-diiodo-

3,6-Diiodopyridazine is an organometallic compound that is used as a palladium-catalyzed cross-coupling reaction. It is a nucleophilic and reacts with electron-deficient alkenes to form trifunctional products. The reaction can be carried out in organic solvents and at room temperature. This compound has been shown to react with cinnolines, luminophors, amines, and diethyl ester to form a variety of functionalities.

CAS 20698-04-8: 3,6-Diiodopyridazine

3,6-Diiodopyridazine

Ref: 54-OR25709

Pyridazine, 3,6-diiodo-

Ref: IN-DA002IRH

3,6-Diiodopyridazine

Ref: TR-D481890

3,6-Diiodopyridazine

Ref: 10-F067468

3,6-Diiodopyridazine

Ref: 3D-FD71567