4-[2,6-Difluoro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine, with the CAS number 1313738-69-0, is a synthetic organic compound characterized by its complex molecular structure, which includes a morpholine ring and a phenyl group substituted with a dioxaborolane moiety. The presence of two fluorine atoms on the phenyl ring enhances its electronic properties, potentially influencing its reactivity and solubility. The dioxaborolane group is notable for its role in various chemical reactions, particularly in organoboron chemistry, where it can participate in cross-coupling reactions. This compound may exhibit unique physical properties such as solubility in organic solvents and specific melting or boiling points, which are influenced by its functional groups. Its applications could span across pharmaceuticals, agrochemicals, or materials science, particularly in the development of novel compounds or intermediates. As with many synthetic compounds, safety and handling precautions are essential due to potential toxicity or reactivity.

4-[2,6-difluoro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine

1313738-69-0: 4-[2,6-Difluoro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine, with the CAS number 1313738-69-0, is a synthetic organic compound characterized by its complex molecular structure, which includes a morpholine ring and a phenyl group substituted with a dioxaborolane moiety. The presence of two fluorine atoms on the phenyl ring enhances its electronic properties, potentially influencing its reactivity and solubility. The dioxaborolane group is notable for its role in various chemical reactions, particularly in organoboron chemistry, where it can participate in cross-coupling reactions. This compound may exhibit unique physical properties such as solubility in organic solvents and specific melting or boiling points, which are influenced by its functional groups. Its applications could span across pharmaceuticals, agrochemicals, or materials science, particularly in the development of novel compounds or intermediates. As with many synthetic compounds, safety and handling precautions are essential due to potential toxicity or reactivity.

Morpholine, 4-[2,6-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-

<p>3,5-Difluoro-4-morpholinophenylboronic Acid Pinacol Ester</p>

CAS 1313738-69-0

4-[2,6-difluoro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]morpholine

Morpholine, 4-[2,6-difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-

Ref: IN-DA000W12

3,5-Difluoro-4-morpholinophenylboronic Acid Pinacol Ester

Ref: 54-PC1003447

4-(2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)morpholine

Ref: 10-F465136