2-(4-Azidobutyl)-1H-isoindole-1,3(2H)-dione, with the CAS number 66917-06-4, is a chemical compound characterized by its isoindole structure, which features a bicyclic system comprising a five-membered ring fused to a six-membered ring. The presence of the azido group (-N3) at the 4-position of the butyl chain introduces notable reactivity, making it a potential candidate for click chemistry applications, particularly in bioconjugation and material science. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its functional groups suggest that it could participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. Safety precautions should be observed when handling this compound due to the inherent reactivity of the azido group, which can be explosive under certain conditions. Overall, 2-(4-azidobutyl)-1H-isoindole-1,3(2H)-dione is of interest in synthetic organic chemistry and materials science for its unique structural features and reactivity.

2-(4-azidobutyl)-1H-isoindole-1,3(2H)-dione

66917-06-4: 2-(4-Azidobutyl)-1H-isoindole-1,3(2H)-dione, with the CAS number 66917-06-4, is a chemical compound characterized by its isoindole structure, which features a bicyclic system comprising a five-membered ring fused to a six-membered ring. The presence of the azido group (-N3) at the 4-position of the butyl chain introduces notable reactivity, making it a potential candidate for click chemistry applications, particularly in bioconjugation and material science. The compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its functional groups suggest that it could participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. Safety precautions should be observed when handling this compound due to the inherent reactivity of the azido group, which can be explosive under certain conditions. Overall, 2-(4-azidobutyl)-1H-isoindole-1,3(2H)-dione is of interest in synthetic organic chemistry and materials science for its unique structural features and reactivity.

CAS 66917-06-4

2-(4-azidobutyl)-1H-isoindole-1,3(2H)-dione

2-(4-azidobutyl)-2,3-dihydro-1H-isoindole-1,3-dione

Ref: 10-F521297