1H-Indazol-6-ol,3-amino- is an organic compound characterized by its indazole core, which consists of a five-membered ring containing two nitrogen atoms. This compound features a hydroxyl group (-OH) at the 6-position and an amino group (-NH2) at the 3-position of the indazole ring, contributing to its reactivity and potential biological activity. The presence of these functional groups suggests that it may participate in hydrogen bonding and can act as both a weak acid and a weak base. The compound is likely to be soluble in polar solvents due to the hydroxyl and amino groups, which can engage in dipole-dipole interactions. Its structure may allow for various applications in medicinal chemistry, particularly in the development of pharmaceuticals, as indazole derivatives are known for their diverse biological activities. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the substituents on the indazole ring, making it a subject of interest for further research in organic synthesis and drug design.

1H-Indazol-6-ol,3-amino-

88805-72-5: 1H-Indazol-6-ol,3-amino- is an organic compound characterized by its indazole core, which consists of a five-membered ring containing two nitrogen atoms. This compound features a hydroxyl group (-OH) at the 6-position and an amino group (-NH2) at the 3-position of the indazole ring, contributing to its reactivity and potential biological activity. The presence of these functional groups suggests that it may participate in hydrogen bonding and can act as both a weak acid and a weak base. The compound is likely to be soluble in polar solvents due to the hydroxyl and amino groups, which can engage in dipole-dipole interactions. Its structure may allow for various applications in medicinal chemistry, particularly in the development of pharmaceuticals, as indazole derivatives are known for their diverse biological activities. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the substituents on the indazole ring, making it a subject of interest for further research in organic synthesis and drug design.

CAS 88805-72-5

1H-Indazol-6-ol,3-amino-

3-Amino-1H-indazol-6-ol

Ref: IN-DA004ASH

3-Amino-1H-indazol-6-ol

Ref: 3D-NDA80572