6-(4-Chlorophenyl)-2-methylpyrimidin-4-amine is an organic compound characterized by its pyrimidine ring structure, which is a six-membered heterocyclic aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a 4-chlorophenyl group at the 6-position and a methyl group at the 2-position contributes to its unique chemical properties. This compound typically exhibits moderate to high solubility in organic solvents, while its solubility in water may vary depending on pH and temperature. It may also display biological activity, making it of interest in pharmaceutical research, particularly in the development of therapeutic agents. The amine functional group can participate in hydrogen bonding, influencing its reactivity and interactions with other molecules. Additionally, the chlorophenyl substituent can affect the compound's electronic properties and lipophilicity, which are important for its potential applications in medicinal chemistry. Overall, this compound's structural features suggest it may have diverse applications in various fields, including drug development and agrochemicals.

6-(4-chlorophenyl)-2-methylpyrimidin-4-amine

91349-35-8: 6-(4-Chlorophenyl)-2-methylpyrimidin-4-amine is an organic compound characterized by its pyrimidine ring structure, which is a six-membered heterocyclic aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a 4-chlorophenyl group at the 6-position and a methyl group at the 2-position contributes to its unique chemical properties. This compound typically exhibits moderate to high solubility in organic solvents, while its solubility in water may vary depending on pH and temperature. It may also display biological activity, making it of interest in pharmaceutical research, particularly in the development of therapeutic agents. The amine functional group can participate in hydrogen bonding, influencing its reactivity and interactions with other molecules. Additionally, the chlorophenyl substituent can affect the compound's electronic properties and lipophilicity, which are important for its potential applications in medicinal chemistry. Overall, this compound's structural features suggest it may have diverse applications in various fields, including drug development and agrochemicals.

CAS 91349-35-8

6-(4-chlorophenyl)-2-methylpyrimidin-4-amine

6-(4-chlorophenyl)-2-methylpyrimidin-4-amine

Ref: IN-DA006NRI

6-(4-CHLOROPHENYL)-2-METHYLPYRIMIDIN-4-AMINE

Ref: 10-F530152