Methyl 2-bromopyrimidine-5-carboxylate is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at the 1 and 3 positions. The presence of a bromine atom at the 2-position and a carboxylate group at the 5-position contributes to its reactivity and potential applications in organic synthesis. The methyl ester functional group enhances its solubility in organic solvents and can participate in various chemical reactions, such as nucleophilic substitutions and esterifications. This compound is often utilized in the synthesis of pharmaceuticals and agrochemicals due to its ability to serve as an intermediate in the formation of more complex molecules. Its properties, including boiling point, melting point, and reactivity, can vary based on the specific conditions and the presence of other functional groups in a reaction. As with many brominated compounds, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and safety measures should be observed due to its potential hazards.

methyl 2-bromopyrimidine-5-carboxylate

1209459-66-4: Methyl 2-bromopyrimidine-5-carboxylate is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at the 1 and 3 positions. The presence of a bromine atom at the 2-position and a carboxylate group at the 5-position contributes to its reactivity and potential applications in organic synthesis. The methyl ester functional group enhances its solubility in organic solvents and can participate in various chemical reactions, such as nucleophilic substitutions and esterifications. This compound is often utilized in the synthesis of pharmaceuticals and agrochemicals due to its ability to serve as an intermediate in the formation of more complex molecules. Its properties, including boiling point, melting point, and reactivity, can vary based on the specific conditions and the presence of other functional groups in a reaction. As with many brominated compounds, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and safety measures should be observed due to its potential hazards.

CAS 1209459-66-4

methyl 2-bromopyrimidine-5-carboxylate

Methyl 2-bromopyrimidine-5-carboxylate

Ref: IN-DA00956W

Methyl 2-bromopyrimidine-5-carboxylate

Ref: 54-OR1049950

Methyl 2-bromopyrimidine-5-carboxylate

Ref: 10-F618903

Methyl 2-bromopyrimidine-5-carboxylate

Ref: 3D-JYB45966