CAS 942185-01-5

1H-pyrazolo[3,4-b]pyridin-5-amine

Description:

1H-pyrazolo[3,4-b]pyridin-5-amine is a heterocyclic organic compound characterized by a fused pyrazole and pyridine ring system. This compound features an amine functional group at the 5-position of the pyrazole ring, which contributes to its reactivity and potential biological activity. It typically exhibits moderate to high solubility in polar solvents due to the presence of the amine group, which can engage in hydrogen bonding. The compound may display interesting pharmacological properties, making it a subject of interest in medicinal chemistry, particularly in the development of new therapeutic agents. Its structure allows for various substitutions, which can influence its biological activity and interaction with target proteins. Additionally, 1H-pyrazolo[3,4-b]pyridin-5-amine may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it a versatile building block in organic synthesis. Overall, this compound's unique structural features and potential applications make it a valuable subject of study in both academic and industrial chemistry contexts.

1H-Pyrazolo[3,4-b]pyridin-5-amine

CAS: 942185-01-5

Formula: C₆H₆N₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 134.1386

Ref: IN-DA00GU9Y

1H-Pyrazolo[3,4-b]pyridin-5-amine

CAS: 942185-01-5

1H-Pyrazolo[3,4-b]pyridin-5-amine

Purity: 98%

Molecular weight: 134.14g/mol

Ref: 54-OR92264

1H-Pyrazolo[3,4-b]pyridin-5-amine

CAS: 942185-01-5

Formula: C₆H₆N₄

Purity: 98%

Color and Shape: No data available.

Molecular weight: 134.142

Ref: 10-F240998

1H-Pyrazolo[3,4-b]pyridin-5-amine

CAS: 942185-01-5

1H-Pyrazolo[3,4-b]pyridin-5-amine is a compound that is soluble in organic solvents and insoluble in water. 1H-Pyrazolo[3,4-b]pyridin-5-amine has been shown to cause the formation of osteoclasts. It has been shown to inhibit the growth of a variety of cancer cells at high concentrations, including breast cancer cells and melanoma cells. This drug also has site specific effects on tumors, which means it will only work on certain sites and not others. The mechanism by which 1H-pyrazolo[3,4-b]pyridin-5-amine causes bone loss is unknown but may involve the regulation of bone cell regulatory proteins.

Formula: C₆H₆N₄

Purity: Min. 95%

Molecular weight: 134.14 g/mol

Ref: 3D-SMB18501