5-Amino-2-[(tetrahydrofuran-2-ylmethyl)amino]benzoic acid is an organic compound characterized by its amino and carboxylic acid functional groups, which contribute to its properties as an amino acid derivative. The presence of the tetrahydrofuran moiety introduces a cyclic ether structure, enhancing its solubility in polar solvents and potentially influencing its biological activity. This compound typically exhibits moderate to high polarity due to the amino and carboxylic acid groups, which can participate in hydrogen bonding. Its molecular structure suggests potential applications in pharmaceuticals, particularly in drug design, where the amino and carboxylic functionalities can facilitate interactions with biological targets. Additionally, the compound may exhibit specific reactivity patterns typical of amino acids, such as undergoing peptide bond formation. The CAS number 896717-80-9 uniquely identifies this substance, allowing for precise reference in chemical databases and literature. Overall, the characteristics of this compound make it a subject of interest in medicinal chemistry and related fields.

5-amino-2-[(tetrahydrofuran-2-ylmethyl)amino]benzoic acid

896717-80-9: 5-Amino-2-[(tetrahydrofuran-2-ylmethyl)amino]benzoic acid is an organic compound characterized by its amino and carboxylic acid functional groups, which contribute to its properties as an amino acid derivative. The presence of the tetrahydrofuran moiety introduces a cyclic ether structure, enhancing its solubility in polar solvents and potentially influencing its biological activity. This compound typically exhibits moderate to high polarity due to the amino and carboxylic acid groups, which can participate in hydrogen bonding. Its molecular structure suggests potential applications in pharmaceuticals, particularly in drug design, where the amino and carboxylic functionalities can facilitate interactions with biological targets. Additionally, the compound may exhibit specific reactivity patterns typical of amino acids, such as undergoing peptide bond formation. The CAS number 896717-80-9 uniquely identifies this substance, allowing for precise reference in chemical databases and literature. Overall, the characteristics of this compound make it a subject of interest in medicinal chemistry and related fields.

CAS 896717-80-9

5-amino-2-[(tetrahydrofuran-2-ylmethyl)amino]benzoic acid

5-Amino-2-(((tetrahydrofuran-2-yl)methyl)amino)benzoic acid

Ref: IN-DA0043SO

5-amino-2-[(tetrahydro-2-furanylmethyl)amino]benzoic acid

Ref: 10-F315499