[4-(Methoxycarbamoyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a methoxycarbamoyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The methoxycarbamoyl group enhances its solubility and reactivity, allowing for potential use in drug development and as a building block in the synthesis of more complex molecules. The compound is likely to be a white to off-white solid, soluble in polar organic solvents, and may exhibit moderate stability under standard laboratory conditions. Its reactivity can be influenced by the presence of the boron atom, which can participate in various chemical reactions, including Suzuki coupling, making it valuable in the formation of carbon-carbon bonds. Overall, [4-(methoxycarbamoyl)phenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry.

[4-(methoxycarbamoyl)phenyl]boronic acid

850568-17-1: [4-(Methoxycarbamoyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a methoxycarbamoyl substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The methoxycarbamoyl group enhances its solubility and reactivity, allowing for potential use in drug development and as a building block in the synthesis of more complex molecules. The compound is likely to be a white to off-white solid, soluble in polar organic solvents, and may exhibit moderate stability under standard laboratory conditions. Its reactivity can be influenced by the presence of the boron atom, which can participate in various chemical reactions, including Suzuki coupling, making it valuable in the formation of carbon-carbon bonds. Overall, [4-(methoxycarbamoyl)phenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry.

CAS 850568-17-1

[4-(methoxycarbamoyl)phenyl]boronic acid

4-(O-Methylhydroxylaminocarbonyl)phenylboronic acid

Ref: IN-DA004PC3

4-(O-Methylhydroxylaminocarbonyl)benzeneboronic acid

Ref: 54-OR3955

(4-(Methoxycarbamoyl)phenyl)boronic acid

Ref: 10-F692517