2-(2-Ethoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique structural features, including a dioxaborolane ring and a trifluoromethyl-substituted aromatic system. The presence of the ethoxy group enhances its solubility in organic solvents, while the trifluoromethyl group contributes to its electronic properties, potentially influencing reactivity and stability. This compound is likely to exhibit interesting chemical behavior due to the boron atom, which can participate in various reactions, including those involving nucleophiles and electrophiles. The dioxaborolane structure is known for its applications in organic synthesis, particularly in the formation of carbon-boron bonds, which are valuable in the development of pharmaceuticals and agrochemicals. Additionally, the steric hindrance provided by the tetramethyl groups may affect the compound's reactivity and interactions with other molecules. Overall, this compound's unique combination of functional groups and structural characteristics makes it a subject of interest in synthetic organic chemistry and materials science.

2-(2-ethoxy-5-(trifluoroMethyl)phenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane

1268511-93-8: 2-(2-Ethoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique structural features, including a dioxaborolane ring and a trifluoromethyl-substituted aromatic system. The presence of the ethoxy group enhances its solubility in organic solvents, while the trifluoromethyl group contributes to its electronic properties, potentially influencing reactivity and stability. This compound is likely to exhibit interesting chemical behavior due to the boron atom, which can participate in various reactions, including those involving nucleophiles and electrophiles. The dioxaborolane structure is known for its applications in organic synthesis, particularly in the formation of carbon-boron bonds, which are valuable in the development of pharmaceuticals and agrochemicals. Additionally, the steric hindrance provided by the tetramethyl groups may affect the compound's reactivity and interactions with other molecules. Overall, this compound's unique combination of functional groups and structural characteristics makes it a subject of interest in synthetic organic chemistry and materials science.

2-(2-Ethoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS 1268511-93-8

2-(2-ethoxy-5-(trifluoroMethyl)phenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane

2-(2-Ethoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Ref: 54-PC1003937