2-Chloro-N-(1-methylethyl)pyrimidin-4-amine, with the CAS number 71406-72-9, is a chemical compound that belongs to the class of pyrimidine derivatives. It features a pyrimidine ring, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. The presence of a chloro group at the 2-position and an isopropyl amine substituent at the 4-position contributes to its unique reactivity and potential biological activity. This compound is typically characterized by its solid state at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. The presence of the chloro substituent may enhance its reactivity in nucleophilic substitution reactions, while the amine group can participate in hydrogen bonding, influencing its interaction with biological targets. As with many pyrimidine derivatives, it may also exhibit interesting pharmacological properties, warranting further investigation in drug discovery contexts.

2-chloro-N-(1-methylethyl)pyrimidin-4-amine

71406-72-9: 2-Chloro-N-(1-methylethyl)pyrimidin-4-amine, with the CAS number 71406-72-9, is a chemical compound that belongs to the class of pyrimidine derivatives. It features a pyrimidine ring, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. The presence of a chloro group at the 2-position and an isopropyl amine substituent at the 4-position contributes to its unique reactivity and potential biological activity. This compound is typically characterized by its solid state at room temperature and may exhibit moderate solubility in polar organic solvents. Its structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. The presence of the chloro substituent may enhance its reactivity in nucleophilic substitution reactions, while the amine group can participate in hydrogen bonding, influencing its interaction with biological targets. As with many pyrimidine derivatives, it may also exhibit interesting pharmacological properties, warranting further investigation in drug discovery contexts.

CAS 71406-72-9

2-chloro-N-(1-methylethyl)pyrimidin-4-amine

2-Chloro-N-isopropylpyrimidin-4-amine

Ref: IN-DA00FDA8

(2-Chloro-pyrimidin-4-yl)-isopropyl-amine

Ref: 10-F088408