4-Chloro-6-ethyl-2-piperidin-1-ylpyrimidine is a chemical compound characterized by its pyrimidine core, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a chloro group at position 4 and an ethyl group at position 6 contributes to its unique reactivity and potential biological activity. The piperidine moiety, attached at position 2, introduces a cyclic amine structure that can enhance the compound's interaction with biological targets, such as receptors or enzymes. This compound may exhibit properties typical of heterocyclic compounds, including potential pharmacological activities, making it of interest in medicinal chemistry. Its molecular structure suggests it could participate in various chemical reactions, including nucleophilic substitutions and electrophilic additions. Additionally, the presence of halogen and alkyl substituents can influence its solubility, stability, and overall reactivity. As with many synthetic organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

4-chloro-6-ethyl-2-piperidin-1-ylpyrimidine

901586-58-1: 4-Chloro-6-ethyl-2-piperidin-1-ylpyrimidine is a chemical compound characterized by its pyrimidine core, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a chloro group at position 4 and an ethyl group at position 6 contributes to its unique reactivity and potential biological activity. The piperidine moiety, attached at position 2, introduces a cyclic amine structure that can enhance the compound's interaction with biological targets, such as receptors or enzymes. This compound may exhibit properties typical of heterocyclic compounds, including potential pharmacological activities, making it of interest in medicinal chemistry. Its molecular structure suggests it could participate in various chemical reactions, including nucleophilic substitutions and electrophilic additions. Additionally, the presence of halogen and alkyl substituents can influence its solubility, stability, and overall reactivity. As with many synthetic organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

CAS 901586-58-1

4-chloro-6-ethyl-2-piperidin-1-ylpyrimidine

4-Chloro-6-ethyl-2-piperidin-1-ylpyrimidine

Ref: IN-DA006HYN

4-chloro-6-ethyl-2-piperidin-1-ylpyrimidine

Ref: 10-F309580