2-Iodo-6-(trifluoromethyl)pyridine is a heterocyclic organic compound characterized by the presence of a pyridine ring substituted at the 2-position with an iodine atom and at the 6-position with a trifluoromethyl group. This compound typically exhibits a pale yellow to light brown appearance and is known for its relatively high stability due to the aromatic nature of the pyridine ring. The trifluoromethyl group contributes to its lipophilicity and can influence its reactivity, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The presence of the iodine atom can facilitate nucleophilic substitution reactions, while the trifluoromethyl group can enhance the compound's biological activity. Additionally, 2-iodo-6-(trifluoromethyl)pyridine may exhibit unique electronic properties due to the electron-withdrawing nature of the trifluoromethyl group, which can affect its interaction with various reagents and biological targets. Safety precautions should be taken when handling this compound, as it may pose health risks and environmental hazards.

2-iodo-6-(trifluoromethyl)pyridine

100366-74-3: 2-Iodo-6-(trifluoromethyl)pyridine is a heterocyclic organic compound characterized by the presence of a pyridine ring substituted at the 2-position with an iodine atom and at the 6-position with a trifluoromethyl group. This compound typically exhibits a pale yellow to light brown appearance and is known for its relatively high stability due to the aromatic nature of the pyridine ring. The trifluoromethyl group contributes to its lipophilicity and can influence its reactivity, making it a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The presence of the iodine atom can facilitate nucleophilic substitution reactions, while the trifluoromethyl group can enhance the compound's biological activity. Additionally, 2-iodo-6-(trifluoromethyl)pyridine may exhibit unique electronic properties due to the electron-withdrawing nature of the trifluoromethyl group, which can affect its interaction with various reagents and biological targets. Safety precautions should be taken when handling this compound, as it may pose health risks and environmental hazards.

CAS 100366-74-3

2-iodo-6-(trifluoromethyl)pyridine

Pyridine, 2-iodo-6-(trifluoromethyl)-

Ref: IN-DA0001PP

2-Iodo-6-(trifluoromethyl)pyridine

Ref: 10-F037268