Tert-butyl (2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethylcarbamate is a chemical compound characterized by its complex structure, which includes a tert-butyl group, a benzodioxin moiety, and a carbamate functional group. This compound is typically used in pharmaceutical and chemical research due to its potential biological activity. The presence of the hydroxyethyl group suggests it may exhibit solubility in polar solvents, while the tert-butyl group can enhance lipophilicity, potentially influencing its pharmacokinetic properties. The benzodioxin structure may contribute to specific interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the stereochemistry indicated by the (2R) designation suggests that the compound has a specific three-dimensional arrangement, which can be crucial for its biological activity and interaction with enzymes or receptors. Overall, this compound's unique structural features may provide insights into its reactivity, stability, and potential applications in drug development or as a chemical probe in biological studies.

tert-butyl (2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethylcarbamate

452339-72-9: Tert-butyl (2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethylcarbamate is a chemical compound characterized by its complex structure, which includes a tert-butyl group, a benzodioxin moiety, and a carbamate functional group. This compound is typically used in pharmaceutical and chemical research due to its potential biological activity. The presence of the hydroxyethyl group suggests it may exhibit solubility in polar solvents, while the tert-butyl group can enhance lipophilicity, potentially influencing its pharmacokinetic properties. The benzodioxin structure may contribute to specific interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the stereochemistry indicated by the (2R) designation suggests that the compound has a specific three-dimensional arrangement, which can be crucial for its biological activity and interaction with enzymes or receptors. Overall, this compound's unique structural features may provide insights into its reactivity, stability, and potential applications in drug development or as a chemical probe in biological studies.

(R)-Tert-Butyl (2-(2,2-Dimethyl-4H-Benzo[D][1,3]Dioxin-6-Yl)-2-Hydroxyethyl)Carbamate

CAS 452339-72-9

tert-butyl (2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethylcarbamate

(R)-Tert-Butyl (2-(2,2-Dimethyl-4H-Benzo[D][1,3]Dioxin-6-Yl)-2-Hydroxyethyl)Carbamate

Ref: 54-OR1027403

Salmeterol Impurity 17

Ref: 4Z-S-1627

tert-Butyl (2R)-2-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-2-hydroxyethylcarbamate

Ref: 10-F789777