1-Benzyl-2-tert-butyl-4-oxopyrazolidine-1,2-dicarboxylate is a chemical compound characterized by its unique pyrazolidine structure, which features a five-membered ring containing two nitrogen atoms. This compound includes a benzyl group and a tert-butyl group, contributing to its hydrophobic characteristics and potentially influencing its solubility and reactivity. The presence of two carboxylate ester functionalities enhances its reactivity, making it a candidate for various chemical transformations. The oxo group (C=O) in the structure indicates that it may participate in reactions typical of carbonyl compounds, such as nucleophilic additions. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the pyrazolidine core, which is known for various biological activities. Additionally, the compound's stability and reactivity can be influenced by the steric hindrance provided by the tert-butyl group, making it an interesting subject for further research in organic synthesis and drug development.

1-benzyl-2-tert-butyl-4-oxopyrazolidine-1,2-dicarboxylate

503072-63-7: 1-Benzyl-2-tert-butyl-4-oxopyrazolidine-1,2-dicarboxylate is a chemical compound characterized by its unique pyrazolidine structure, which features a five-membered ring containing two nitrogen atoms. This compound includes a benzyl group and a tert-butyl group, contributing to its hydrophobic characteristics and potentially influencing its solubility and reactivity. The presence of two carboxylate ester functionalities enhances its reactivity, making it a candidate for various chemical transformations. The oxo group (C=O) in the structure indicates that it may participate in reactions typical of carbonyl compounds, such as nucleophilic additions. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the pyrazolidine core, which is known for various biological activities. Additionally, the compound's stability and reactivity can be influenced by the steric hindrance provided by the tert-butyl group, making it an interesting subject for further research in organic synthesis and drug development.

CAS 503072-63-7

1-benzyl-2-tert-butyl-4-oxopyrazolidine-1,2-dicarboxylate

1-BENZYL 2-TERT-BUTYL 4-OXOPYRAZOLIDINE-1,2-DICARBOXYLATE

Ref: 10-F390309