[2-(Aminomethyl)-5-fluorophenyl]boronic acid hydrochloride is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that features both an amino group and a fluorine atom. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and methanol, which is a common trait for boronic acids due to their ability to form hydrogen bonds. The amino group contributes to its basicity, while the fluorine atom can influence its electronic properties and reactivity. This compound is often utilized in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals and as a building block in the synthesis of more complex molecules. Its boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the formation of carbon-carbon bonds. Additionally, the hydrochloride salt form enhances its stability and solubility, facilitating its use in various chemical applications.

[2-(aminomethyl)-5-fluorophenyl]boronic acid hydrochloride

850568-03-5: [2-(Aminomethyl)-5-fluorophenyl]boronic acid hydrochloride is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that features both an amino group and a fluorine atom. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and methanol, which is a common trait for boronic acids due to their ability to form hydrogen bonds. The amino group contributes to its basicity, while the fluorine atom can influence its electronic properties and reactivity. This compound is often utilized in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals and as a building block in the synthesis of more complex molecules. Its boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the formation of carbon-carbon bonds. Additionally, the hydrochloride salt form enhances its stability and solubility, facilitating its use in various chemical applications.

CAS 850568-03-5

[2-(aminomethyl)-5-fluorophenyl]boronic acid hydrochloride

(2-(Aminomethyl)-5-Fluorophenyl)Boronic Acid Hydrochloride

Ref: IN-DA004PC8

2-(Aminomethyl)-5-fluorobenzeneboronic acid hydrochloride

Ref: 54-PC2668

(2-(Aminomethyl)-5-fluorophenyl)boronic acid hydrochloride

Ref: 10-F219861