The chemical substance known as [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]acetonitrile, with the CAS number 475272-13-0, is characterized by its unique structural features that include a phenoxy group and a dioxaborolane moiety. This compound typically exhibits properties associated with both organic and boron-containing compounds, such as potential reactivity in nucleophilic substitution reactions due to the presence of the acetonitrile functional group. The dioxaborolane ring contributes to its stability and may enhance its solubility in organic solvents. Additionally, the presence of the tetramethyl substituents can influence its steric properties, potentially affecting its reactivity and interactions with other molecules. This compound may find applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals, owing to the versatile reactivity of boron-containing compounds. Its specific physical properties, such as melting point, boiling point, and solubility, would need to be determined experimentally or sourced from reliable chemical databases for precise applications.

[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]acetonitrile

475272-13-0: The chemical substance known as [4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]acetonitrile, with the CAS number 475272-13-0, is characterized by its unique structural features that include a phenoxy group and a dioxaborolane moiety. This compound typically exhibits properties associated with both organic and boron-containing compounds, such as potential reactivity in nucleophilic substitution reactions due to the presence of the acetonitrile functional group. The dioxaborolane ring contributes to its stability and may enhance its solubility in organic solvents. Additionally, the presence of the tetramethyl substituents can influence its steric properties, potentially affecting its reactivity and interactions with other molecules. This compound may find applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals, owing to the versatile reactivity of boron-containing compounds. Its specific physical properties, such as melting point, boiling point, and solubility, would need to be determined experimentally or sourced from reliable chemical databases for precise applications.

CAS 475272-13-0

[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]acetonitrile

4-CYANOMETHOXY-PHENYLBORONIC ACID, PINACOL ESTER

Ref: IN-DA00700K

4-Cyanomethoxyphenylboronic acid, pinacol ester

Ref: 54-OR361030

2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetonitrile

Ref: 10-F694089