Ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate is a chemical compound characterized by its unique pyrazolo-pyrimidine structure, which incorporates a bromine atom at the 5-position of the pyrazole ring. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of the carboxylate group enhances its potential for various chemical reactions, including esterification and nucleophilic substitutions. Ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate is of interest in medicinal chemistry due to its potential biological activity, particularly in the development of pharmaceuticals targeting specific pathways. Its molecular structure suggests possible interactions with biological macromolecules, making it a candidate for further research in drug discovery. Additionally, the bromine substituent may influence the compound's electronic properties and reactivity, which can be advantageous in synthetic applications. Overall, this compound exemplifies the diverse chemistry of heterocyclic compounds and their utility in various scientific fields.

ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate

1436686-17-7: Ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate is a chemical compound characterized by its unique pyrazolo-pyrimidine structure, which incorporates a bromine atom at the 5-position of the pyrazole ring. This compound features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of the carboxylate group enhances its potential for various chemical reactions, including esterification and nucleophilic substitutions. Ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate is of interest in medicinal chemistry due to its potential biological activity, particularly in the development of pharmaceuticals targeting specific pathways. Its molecular structure suggests possible interactions with biological macromolecules, making it a candidate for further research in drug discovery. Additionally, the bromine substituent may influence the compound's electronic properties and reactivity, which can be advantageous in synthetic applications. Overall, this compound exemplifies the diverse chemistry of heterocyclic compounds and their utility in various scientific fields.

CAS 1436686-17-7

ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate

Ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate

Ref: IN-DA00AO9G

Ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate

Ref: 54-OR76440

Ethyl 5-bromopyrazolo[1,5-a]pyrimidine-3-carboxylate

Ref: 10-F455408