N-(2-Amino-6-chloro-4-pyrimidinyl)-N-benzylamine, with the CAS number 91066-67-0, is a chemical compound characterized by its pyrimidine and amine functional groups. This substance features a pyrimidine ring substituted with an amino group and a chlorine atom at specific positions, contributing to its biological activity. The benzylamine moiety enhances its lipophilicity, potentially influencing its interaction with biological targets. Typically, compounds of this nature may exhibit properties such as moderate solubility in organic solvents and varying solubility in water, depending on the pH of the solution. The presence of both amino and chlorinated groups suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. Additionally, the compound may exhibit specific reactivity patterns due to the functional groups present, making it a candidate for further chemical modifications or as a precursor in synthetic pathways. As with many organic compounds, safety and handling precautions should be observed, given the potential for biological activity and toxicity associated with amine and halogenated compounds.

N-(2-AMINO-6-CHLORO-4-PYRIMIDINYL)-N-BENZYLAMINE

91066-67-0: N-(2-Amino-6-chloro-4-pyrimidinyl)-N-benzylamine, with the CAS number 91066-67-0, is a chemical compound characterized by its pyrimidine and amine functional groups. This substance features a pyrimidine ring substituted with an amino group and a chlorine atom at specific positions, contributing to its biological activity. The benzylamine moiety enhances its lipophilicity, potentially influencing its interaction with biological targets. Typically, compounds of this nature may exhibit properties such as moderate solubility in organic solvents and varying solubility in water, depending on the pH of the solution. The presence of both amino and chlorinated groups suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. Additionally, the compound may exhibit specific reactivity patterns due to the functional groups present, making it a candidate for further chemical modifications or as a precursor in synthetic pathways. As with many organic compounds, safety and handling precautions should be observed, given the potential for biological activity and toxicity associated with amine and halogenated compounds.

CAS 91066-67-0

N-(2-AMINO-6-CHLORO-4-PYRIMIDINYL)-N-BENZYLAMINE

N~4~-benzyl-6-chloropyrimidine-2,4-diamine

Ref: 10-F373164