Pyridazin-4-ylboronic acid is an organic compound characterized by the presence of a pyridazine ring, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 2, and a boronic acid functional group (-B(OH)2) at the 4-position. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols due to the presence of the boronic acid group, which can form hydrogen bonds. Pyridazin-4-ylboronic acid is notable for its ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and materials science. It can serve as a building block in the synthesis of more complex molecules and is often employed in the development of pharmaceuticals, particularly in the context of targeted drug delivery and as a tool in chemical biology. Additionally, its boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, a key method in organic synthesis.

Pyridazin-4-ylboronic acid

1083326-29-7: Pyridazin-4-ylboronic acid is an organic compound characterized by the presence of a pyridazine ring, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 2, and a boronic acid functional group (-B(OH)2) at the 4-position. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols due to the presence of the boronic acid group, which can form hydrogen bonds. Pyridazin-4-ylboronic acid is notable for its ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and materials science. It can serve as a building block in the synthesis of more complex molecules and is often employed in the development of pharmaceuticals, particularly in the context of targeted drug delivery and as a tool in chemical biology. Additionally, its boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, a key method in organic synthesis.

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CAS 1083326-29-7

Pyridazin-4-ylboronic acid

Pyridazin-4-ylboronic acid

Ref: IN-DA00HB5N

Pyridazin-4-ylboronic acid

Ref: 3D-FP178383