4-Chloro-2-methyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine is a heterocyclic organic compound characterized by its complex bicyclic structure, which incorporates both pyridine and pyrimidine rings. This compound features a chlorine atom at the 4-position and a methyl group at the 2-position of the pyridine ring, contributing to its unique chemical properties. The tetrahydropyrido structure indicates that the compound has undergone partial hydrogenation, resulting in a saturated framework that enhances its stability and reactivity. Typically, such compounds may exhibit biological activity, making them of interest in medicinal chemistry and drug development. The presence of halogen substituents, like chlorine, often influences the compound's lipophilicity and potential interactions with biological targets. Additionally, the molecular structure suggests potential for various chemical reactions, including nucleophilic substitutions and cyclization, which can be exploited in synthetic organic chemistry. Overall, 4-chloro-2-methyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine represents a versatile scaffold for further chemical exploration and application.

4-chloro-2-methyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine

944901-71-7: 4-Chloro-2-methyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine is a heterocyclic organic compound characterized by its complex bicyclic structure, which incorporates both pyridine and pyrimidine rings. This compound features a chlorine atom at the 4-position and a methyl group at the 2-position of the pyridine ring, contributing to its unique chemical properties. The tetrahydropyrido structure indicates that the compound has undergone partial hydrogenation, resulting in a saturated framework that enhances its stability and reactivity. Typically, such compounds may exhibit biological activity, making them of interest in medicinal chemistry and drug development. The presence of halogen substituents, like chlorine, often influences the compound's lipophilicity and potential interactions with biological targets. Additionally, the molecular structure suggests potential for various chemical reactions, including nucleophilic substitutions and cyclization, which can be exploited in synthetic organic chemistry. Overall, 4-chloro-2-methyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine represents a versatile scaffold for further chemical exploration and application.

CAS 944901-71-7

4-chloro-2-methyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine

4-Chloro-2-methyl-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine

Ref: 10-F603863