Tert-butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopent-3-en-1-yl)carbamate is a chemical compound characterized by its complex structure, which includes a tert-butyl group, a cyclopentene moiety, and a dioxaborolane unit. The presence of the carbamate functional group indicates that it can participate in various chemical reactions, including hydrolysis and transesterification. This compound is likely to exhibit moderate polarity due to the presence of both hydrophobic (tert-butyl) and hydrophilic (carbamate and dioxaborolane) components. Its dioxaborolane structure suggests potential applications in organic synthesis, particularly in the formation of boron-containing compounds, which are valuable in various chemical transformations. Additionally, the cyclopentene ring may impart unique reactivity, making it suitable for further functionalization. The compound's stability and reactivity can be influenced by environmental factors such as temperature and pH. Overall, this substance represents a versatile building block in organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.

tert-butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopent-3-en-1-yl)carbamate

1643574-07-5: Tert-butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopent-3-en-1-yl)carbamate is a chemical compound characterized by its complex structure, which includes a tert-butyl group, a cyclopentene moiety, and a dioxaborolane unit. The presence of the carbamate functional group indicates that it can participate in various chemical reactions, including hydrolysis and transesterification. This compound is likely to exhibit moderate polarity due to the presence of both hydrophobic (tert-butyl) and hydrophilic (carbamate and dioxaborolane) components. Its dioxaborolane structure suggests potential applications in organic synthesis, particularly in the formation of boron-containing compounds, which are valuable in various chemical transformations. Additionally, the cyclopentene ring may impart unique reactivity, making it suitable for further functionalization. The compound's stability and reactivity can be influenced by environmental factors such as temperature and pH. Overall, this substance represents a versatile building block in organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.

CAS 1643574-07-5

tert-butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopent-3-en-1-yl)carbamate

tert-Butyl (3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopent-3-en-1-yl)carbamate

Ref: 3D-TQC57407