6-Amino-3-iodo-5-nitropyridin-2(1H)-one is a heterocyclic organic compound characterized by its pyridine ring structure, which contains various functional groups that contribute to its chemical properties. The presence of an amino group (-NH2) at the 6-position, an iodo group (-I) at the 3-position, and a nitro group (-NO2) at the 5-position makes this compound a versatile intermediate in organic synthesis. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group. The nitro group is known for its electron-withdrawing properties, which can influence the reactivity of the compound in electrophilic substitution reactions. Additionally, the iodine atom can participate in nucleophilic substitution reactions, making this compound useful in various chemical transformations. Its unique combination of functional groups may also impart biological activity, making it of interest in pharmaceutical research. Safety precautions should be taken when handling this compound, as it may pose health risks associated with its nitro and iodo functionalities.

6-amino-3-iodo-5-nitropyridin-2(1H)-one

642460-96-6: 6-Amino-3-iodo-5-nitropyridin-2(1H)-one is a heterocyclic organic compound characterized by its pyridine ring structure, which contains various functional groups that contribute to its chemical properties. The presence of an amino group (-NH2) at the 6-position, an iodo group (-I) at the 3-position, and a nitro group (-NO2) at the 5-position makes this compound a versatile intermediate in organic synthesis. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group. The nitro group is known for its electron-withdrawing properties, which can influence the reactivity of the compound in electrophilic substitution reactions. Additionally, the iodine atom can participate in nucleophilic substitution reactions, making this compound useful in various chemical transformations. Its unique combination of functional groups may also impart biological activity, making it of interest in pharmaceutical research. Safety precautions should be taken when handling this compound, as it may pose health risks associated with its nitro and iodo functionalities.

CAS 642460-96-6

6-amino-3-iodo-5-nitropyridin-2(1H)-one

2(1H)-Pyridinone, 6-amino-3-iodo-5-nitro-

Ref: IN-DA00ECBU

6-Amino-3-iodo-5-nitro-1h-pyridin-2-one

Ref: 10-F787829