Tert-butyl 1H-indazol-5-ylcarbamate, identified by its CAS number 917474-59-0, is a chemical compound characterized by its unique structure, which includes an indazole ring and a carbamate functional group. This compound typically exhibits properties associated with both organic and medicinal chemistry, making it of interest in various research applications. It is generally a solid at room temperature and may be soluble in organic solvents, depending on the specific conditions. The tert-butyl group contributes to its hydrophobic characteristics, potentially influencing its biological activity and interactions. The indazole moiety is known for its presence in various pharmacologically active compounds, suggesting that tert-butyl 1H-indazol-5-ylcarbamate may possess interesting biological properties. Additionally, the carbamate group can participate in hydrogen bonding, which may affect its reactivity and stability. Overall, this compound's structural features suggest potential utility in drug development and other chemical applications, although specific biological activities would require further investigation.

tert-butyl 1H-indazol-5-ylcarbamate

917474-59-0: Tert-butyl 1H-indazol-5-ylcarbamate, identified by its CAS number 917474-59-0, is a chemical compound characterized by its unique structure, which includes an indazole ring and a carbamate functional group. This compound typically exhibits properties associated with both organic and medicinal chemistry, making it of interest in various research applications. It is generally a solid at room temperature and may be soluble in organic solvents, depending on the specific conditions. The tert-butyl group contributes to its hydrophobic characteristics, potentially influencing its biological activity and interactions. The indazole moiety is known for its presence in various pharmacologically active compounds, suggesting that tert-butyl 1H-indazol-5-ylcarbamate may possess interesting biological properties. Additionally, the carbamate group can participate in hydrogen bonding, which may affect its reactivity and stability. Overall, this compound's structural features suggest potential utility in drug development and other chemical applications, although specific biological activities would require further investigation.

CAS 917474-59-0

tert-butyl 1H-indazol-5-ylcarbamate

5-BOC-AMINOINDAZOLE

Ref: IN-DA00H29Z

tert-Butyl 1H-indazol-5-ylcarbamate

Ref: 54-OR1064602