3-Bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidin-6-amine is a heterocyclic compound characterized by its complex structure, which includes a pyrazolo-pyrimidine framework. This compound features a bromine atom at the 3-position and a chlorine atom at the 4-position of the pyrazolo ring, along with an amino group at the 6-position. The presence of these halogen substituents can influence its reactivity and solubility, making it of interest in medicinal chemistry and drug development. The compound is typically synthesized through multi-step organic reactions, often involving halogenation and amination processes. Its unique structure may exhibit biological activity, potentially serving as a scaffold for the development of pharmaceuticals targeting various diseases. Additionally, the compound's properties, such as melting point, solubility, and spectral characteristics, are essential for understanding its behavior in different environments and applications. As with many heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, further expanding its utility in synthetic chemistry.

3-bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidin-6-amine

1003298-79-0: 3-Bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidin-6-amine is a heterocyclic compound characterized by its complex structure, which includes a pyrazolo-pyrimidine framework. This compound features a bromine atom at the 3-position and a chlorine atom at the 4-position of the pyrazolo ring, along with an amino group at the 6-position. The presence of these halogen substituents can influence its reactivity and solubility, making it of interest in medicinal chemistry and drug development. The compound is typically synthesized through multi-step organic reactions, often involving halogenation and amination processes. Its unique structure may exhibit biological activity, potentially serving as a scaffold for the development of pharmaceuticals targeting various diseases. Additionally, the compound's properties, such as melting point, solubility, and spectral characteristics, are essential for understanding its behavior in different environments and applications. As with many heterocycles, it may also participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, further expanding its utility in synthetic chemistry.

6-Amino-3-bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidine

CAS 1003298-79-0

3-bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidin-6-amine

3-bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidin-6-amine

Ref: IN-DA0001M9

6-Amino-3-bromo-4-chloro-1H-pyrazolo[3,4-d]pyrimidine

Ref: 54-OR18021