2-Chloro-5-fluoro-4-iodo-3-methyl-pyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with various halogen and methyl groups. The presence of chlorine, fluorine, and iodine atoms introduces significant polarity and reactivity, making this compound of interest in medicinal chemistry and material science. The methyl group at the 3-position contributes to the compound's overall hydrophobic character, while the halogen substituents can influence its electronic properties and reactivity. This compound may exhibit unique biological activities due to its structural features, potentially serving as a scaffold for drug development. Its CAS number, 884494-50-2, allows for easy identification in chemical databases. In terms of physical properties, it is likely to be a solid at room temperature, with solubility varying depending on the solvent used. The compound's synthesis typically involves halogenation and methylation reactions, and it may be analyzed using techniques such as NMR spectroscopy, mass spectrometry, and chromatography to confirm its structure and purity.

2-chloro-5-fluoro-4-iodo-3-methyl-pyridine

884494-50-2: 2-Chloro-5-fluoro-4-iodo-3-methyl-pyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with various halogen and methyl groups. The presence of chlorine, fluorine, and iodine atoms introduces significant polarity and reactivity, making this compound of interest in medicinal chemistry and material science. The methyl group at the 3-position contributes to the compound's overall hydrophobic character, while the halogen substituents can influence its electronic properties and reactivity. This compound may exhibit unique biological activities due to its structural features, potentially serving as a scaffold for drug development. Its CAS number, 884494-50-2, allows for easy identification in chemical databases. In terms of physical properties, it is likely to be a solid at room temperature, with solubility varying depending on the solvent used. The compound's synthesis typically involves halogenation and methylation reactions, and it may be analyzed using techniques such as NMR spectroscopy, mass spectrometry, and chromatography to confirm its structure and purity.

CAS 884494-50-2

2-chloro-5-fluoro-4-iodo-3-methyl-pyridine

2-CHLORO-5-FLUORO-4-IODO-3-PICOLINE

Ref: IN-DA00GSKI

2-Chloro-5-fluoro-4-iodo-3-methylpyridine

Ref: 54-PC110961

2-CHLORO-5-FLUORO-4-IODO-3-METHYLPYRIDINE

Ref: 10-F858705