3-Chloro-2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound characterized by its complex structure, which includes a pyridine ring substituted with a chloro group and a methoxy group, as well as a boron-containing moiety. The presence of the chloro group suggests potential reactivity in nucleophilic substitution reactions, while the methoxy group can influence the compound's polarity and solubility. The boron-containing dioxaborolane unit is notable for its role in various organic transformations, particularly in cross-coupling reactions, making this compound potentially useful in synthetic organic chemistry. The steric bulk provided by the tetramethyl groups enhances the stability of the boron moiety, which can affect its reactivity. Overall, this compound may exhibit interesting properties in terms of reactivity, solubility, and potential applications in medicinal chemistry or materials science, although specific behaviors would depend on the context of its use and the conditions under which it is studied.

3-chloro-2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1073353-73-7: 3-Chloro-2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a chemical compound characterized by its complex structure, which includes a pyridine ring substituted with a chloro group and a methoxy group, as well as a boron-containing moiety. The presence of the chloro group suggests potential reactivity in nucleophilic substitution reactions, while the methoxy group can influence the compound's polarity and solubility. The boron-containing dioxaborolane unit is notable for its role in various organic transformations, particularly in cross-coupling reactions, making this compound potentially useful in synthetic organic chemistry. The steric bulk provided by the tetramethyl groups enhances the stability of the boron moiety, which can affect its reactivity. Overall, this compound may exhibit interesting properties in terms of reactivity, solubility, and potential applications in medicinal chemistry or materials science, although specific behaviors would depend on the context of its use and the conditions under which it is studied.

CAS 1073353-73-7

3-chloro-2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

3-Chloro-2-methoxypyridine-4-boronic acid, pinacol ester

Ref: IN-DA003J72

3-Chloro-2-methoxypyridine-4-boronic acid, pinacol ester

Ref: 54-OR360960

3-Chloro-2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Ref: 10-F228476