1-Butyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea, identified by CAS number 850567-59-8, is a chemical compound that features a urea functional group linked to a butyl chain and a phenyl group substituted with a boron-containing moiety. This compound is characterized by its unique structure, which includes a dioxaborolane ring that enhances its reactivity and potential applications in organic synthesis and materials science. The presence of the butyl group contributes to its hydrophobic properties, while the urea functionality can engage in hydrogen bonding, influencing its solubility and interaction with other molecules. The compound may exhibit interesting properties such as fluorescence or catalytic activity, depending on its specific application. Its stability and reactivity can be influenced by the steric and electronic effects of the substituents, making it a subject of interest in various fields, including medicinal chemistry and polymer science. Overall, this compound represents a versatile building block for further chemical modifications and applications.

1-butyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea

850567-59-8: 1-Butyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea, identified by CAS number 850567-59-8, is a chemical compound that features a urea functional group linked to a butyl chain and a phenyl group substituted with a boron-containing moiety. This compound is characterized by its unique structure, which includes a dioxaborolane ring that enhances its reactivity and potential applications in organic synthesis and materials science. The presence of the butyl group contributes to its hydrophobic properties, while the urea functionality can engage in hydrogen bonding, influencing its solubility and interaction with other molecules. The compound may exhibit interesting properties such as fluorescence or catalytic activity, depending on its specific application. Its stability and reactivity can be influenced by the steric and electronic effects of the substituents, making it a subject of interest in various fields, including medicinal chemistry and polymer science. Overall, this compound represents a versatile building block for further chemical modifications and applications.

CAS 850567-59-8

1-butyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea

4-(3-Butylureido)phenylboronic acid, pinacol ester

Ref: IN-DA004Z7W

4-[(But-1-ylcarbamoyl)amino]benzeneboronic acid, pinacol ester

Ref: 54-OR4122

1-Butyl-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea

Ref: 10-F694252