2,6-Bis(chloromethyl)pyridine, with the CAS number 3099-28-3, is a chemical compound characterized by its pyridine ring substituted with two chloromethyl groups at the 2 and 6 positions. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its form and purity. It is known for its reactivity due to the presence of chloromethyl groups, which can undergo nucleophilic substitution reactions, making it useful in organic synthesis and as an intermediate in the production of various pharmaceuticals and agrochemicals. The compound is moderately soluble in organic solvents but has limited solubility in water. Safety considerations are important when handling this substance, as it can be irritating to the skin, eyes, and respiratory system, and appropriate precautions should be taken to minimize exposure. Additionally, it is essential to store it in a cool, dry place away from incompatible materials to ensure stability and safety.

2,6-Bis(chloromethyl)pyridine

2,6-Bis(Chloromethyl)pyridine (BMP) is a molecule with two chlorine atoms that has been synthesized in the form of a crystalline solid. It has an asymmetric tetranuclear structure and consists of four chloride ions and two pyridine rings linked by hydrogen bonds. The molecule can be described as a chelate ring with coordination chemistry involving six ligands, including two water molecules. The crystal structures of BMP have been determined using x-ray diffraction. The vibrational spectra of the molecule have been studied from the ultraviolet to infrared regions. The thermal decomposition temperature of BMP is about 140°C at atmospheric pressure and it can be hydrolyzed by hydrochloric acid or metathesis reactions.

CAS 3099-28-3: 2,6-Bis(chloromethyl)pyridine

2,6-Bis(Chloromethyl)Pyridine

Ref: 3D-FB74917

2,6-Bis(chloromethyl)pyridine

Ref: 54-OR919509

Pyridine, 2,6-bis(chloromethyl)-

Ref: IN-DA0031UY

2,6-Bis(chloromethyl)pyridine

Ref: 3B-B1449

2,6-Bis(chloromethyl)pyridine

Ref: 10-F234930