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CAS 1201790-19-3

:

{3-[4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-propyl}-carbamic acid tert-butyl ester

Description:
The chemical substance known as {3-[4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-propyl}-carbamic acid tert-butyl ester is characterized by its complex structure, which includes a carbamic acid moiety and a tert-butyl ester group. The presence of the dioxaborolane ring suggests potential applications in organic synthesis and medicinal chemistry, particularly in the context of boron-containing compounds that can participate in various chemical reactions, such as Suzuki coupling. The phenoxy group contributes to the compound's hydrophobic characteristics, while the propyl chain enhances its solubility in organic solvents. This compound may exhibit biological activity due to its structural features, making it of interest in pharmaceutical research. Additionally, the tert-butyl ester group can influence the compound's stability and reactivity, potentially affecting its pharmacokinetic properties. Overall, this substance represents a unique combination of functional groups that may provide valuable properties for various applications in chemistry and biology.
Formula:C20H32BNO5
Synonyms:
  • {3-[4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenoxy]-propyl}-carbamic acid tert-butyl ester
  • tert-Butyl (3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)propyl)carbamate
  • Carbamic acid, N-[3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]propyl]-, 1,1-dimethylethyl ester
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