Methyl (2E)-3-(pyrimidin-5-yl)prop-2-enoate is an organic compound characterized by its ester functional group and a pyrimidine ring. The structure features a prop-2-enoate backbone, which includes a double bond between the second and third carbon atoms, contributing to its reactivity and potential for polymerization. The presence of the pyrimidine moiety, a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3, imparts unique chemical properties, including potential interactions with biological targets. This compound is likely to exhibit moderate polarity due to the ester and nitrogen-containing heterocycle, influencing its solubility in various solvents. Additionally, it may participate in various chemical reactions, such as nucleophilic substitutions or additions, due to the electrophilic nature of the double bond. Methyl (2E)-3-(pyrimidin-5-yl)prop-2-enoate may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, owing to the biological significance of pyrimidine derivatives. Its specific reactivity and interactions would depend on the surrounding chemical environment and conditions.

methyl (2E)-3-(pyrimidin-5-yl)prop-2-enoate

866621-24-1: Methyl (2E)-3-(pyrimidin-5-yl)prop-2-enoate is an organic compound characterized by its ester functional group and a pyrimidine ring. The structure features a prop-2-enoate backbone, which includes a double bond between the second and third carbon atoms, contributing to its reactivity and potential for polymerization. The presence of the pyrimidine moiety, a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3, imparts unique chemical properties, including potential interactions with biological targets. This compound is likely to exhibit moderate polarity due to the ester and nitrogen-containing heterocycle, influencing its solubility in various solvents. Additionally, it may participate in various chemical reactions, such as nucleophilic substitutions or additions, due to the electrophilic nature of the double bond. Methyl (2E)-3-(pyrimidin-5-yl)prop-2-enoate may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, owing to the biological significance of pyrimidine derivatives. Its specific reactivity and interactions would depend on the surrounding chemical environment and conditions.

CAS 866621-24-1

methyl (2E)-3-(pyrimidin-5-yl)prop-2-enoate

Methyl 3-(pyrimidin-5-yl)acrylate

Ref: 54-OR301198

(E)-METHYL 3-(PYRIMIDIN-5-YL)ACRYLATE

Ref: 10-F386568