3-Amino-4-borono-benzoic acid hydrochloride is a chemical compound characterized by its boronic acid functionality, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in medicinal chemistry and organic synthesis. The presence of an amino group enhances its solubility in water and its reactivity in biological systems. As a hydrochloride salt, it is typically more stable and easier to handle than its free acid form. This compound is often utilized in the development of pharmaceuticals, especially in the synthesis of compounds that target specific biological pathways. Its boron atom can participate in various chemical reactions, including Suzuki coupling, which is significant in the formation of carbon-carbon bonds. The compound's structure includes a benzene ring, which contributes to its aromatic properties, and the presence of both amino and boronic acid groups allows for diverse interactions in chemical and biological contexts. Overall, 3-amino-4-borono-benzoic acid hydrochloride is a versatile compound with important implications in research and development.

3-amino-4-borono-benzoic acid hydrochloride

850568-60-4: 3-Amino-4-borono-benzoic acid hydrochloride is a chemical compound characterized by its boronic acid functionality, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, particularly in medicinal chemistry and organic synthesis. The presence of an amino group enhances its solubility in water and its reactivity in biological systems. As a hydrochloride salt, it is typically more stable and easier to handle than its free acid form. This compound is often utilized in the development of pharmaceuticals, especially in the synthesis of compounds that target specific biological pathways. Its boron atom can participate in various chemical reactions, including Suzuki coupling, which is significant in the formation of carbon-carbon bonds. The compound's structure includes a benzene ring, which contributes to its aromatic properties, and the presence of both amino and boronic acid groups allows for diverse interactions in chemical and biological contexts. Overall, 3-amino-4-borono-benzoic acid hydrochloride is a versatile compound with important implications in research and development.

2-Amino-4-carboxylphenylboronic acid , HCl

2-Amino-4-carboxybenzeneboronic acid hydrochloride

CAS 850568-60-4

3-amino-4-borono-benzoic acid hydrochloride

2-Amino-4-carboxylphenylboronic acid , HCl

Ref: IN-DA004Z7K

2-Amino-4-carboxybenzeneboronic acid hydrochloride

Ref: 54-OR1934