Ethyl 2-(chloromethyl)pyrimidine-4-carboxylate is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. This compound features a carboxylate group, which contributes to its acidic properties, and an ethyl ester moiety that enhances its solubility in organic solvents. The presence of a chloromethyl group at the 2-position of the pyrimidine ring introduces a reactive site, making it useful in various synthetic applications, particularly in medicinal chemistry for the development of pharmaceuticals. The compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its reactivity can be influenced by the presence of the chlorine atom, which can participate in nucleophilic substitution reactions. Ethyl 2-(chloromethyl)pyrimidine-4-carboxylate is of interest in research due to its potential biological activity and utility in the synthesis of more complex organic molecules. Safety data should be consulted for handling and storage, as halogenated compounds can pose health risks.

ethyl 2-(chloromethyl)pyrimidine-4-carboxylate

944899-56-3: Ethyl 2-(chloromethyl)pyrimidine-4-carboxylate is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. This compound features a carboxylate group, which contributes to its acidic properties, and an ethyl ester moiety that enhances its solubility in organic solvents. The presence of a chloromethyl group at the 2-position of the pyrimidine ring introduces a reactive site, making it useful in various synthetic applications, particularly in medicinal chemistry for the development of pharmaceuticals. The compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions. Its reactivity can be influenced by the presence of the chlorine atom, which can participate in nucleophilic substitution reactions. Ethyl 2-(chloromethyl)pyrimidine-4-carboxylate is of interest in research due to its potential biological activity and utility in the synthesis of more complex organic molecules. Safety data should be consulted for handling and storage, as halogenated compounds can pose health risks.

CAS 944899-56-3

ethyl 2-(chloromethyl)pyrimidine-4-carboxylate

Ethyl 2-(chloromethyl)pyrimidine-4-carboxylate

Ref: IN-DA00II8M