1-Boc-3-aminoindazole is a chemical compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. The "1-Boc" designation indicates the presence of a tert-butyloxycarbonyl (Boc) protecting group at the nitrogen atom in the 1-position of the indazole, which is commonly used in organic synthesis to protect amines during reactions. The "3-amino" part signifies that there is an amino group (-NH2) at the 3-position of the indazole ring. This compound is typically utilized in medicinal chemistry and drug development due to its potential biological activity. It may exhibit properties such as being a building block for more complex molecules or serving as a pharmacophore in drug design. The presence of both the Boc group and the amino group allows for further functionalization and modification, making it a versatile intermediate in synthetic pathways. As with many organic compounds, its solubility, stability, and reactivity can vary based on the conditions and solvents used.

1-Boc-3-aminoindazole

1204298-58-7: 1-Boc-3-aminoindazole is a chemical compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. The "1-Boc" designation indicates the presence of a tert-butyloxycarbonyl (Boc) protecting group at the nitrogen atom in the 1-position of the indazole, which is commonly used in organic synthesis to protect amines during reactions. The "3-amino" part signifies that there is an amino group (-NH2) at the 3-position of the indazole ring. This compound is typically utilized in medicinal chemistry and drug development due to its potential biological activity. It may exhibit properties such as being a building block for more complex molecules or serving as a pharmacophore in drug design. The presence of both the Boc group and the amino group allows for further functionalization and modification, making it a versatile intermediate in synthetic pathways. As with many organic compounds, its solubility, stability, and reactivity can vary based on the conditions and solvents used.

tert-Butyl 3-amino-1H-indazole-1-carboxylate

CAS 1204298-58-7

1-Boc-3-aminoindazole

1-Boc-3-aminoindazole

Ref: IN-DA008UQ2

tert-Butyl 3-amino-1H-indazole-1-carboxylate

Ref: 54-OR78161

tert-Butyl 3-amino-1H-indazole-1-carboxylate

Ref: 10-F224850