Tert-butyl 6-nitroindoline-1-carboxylate is an organic compound characterized by its indoline structure, which features a nitro group and a tert-butyl ester functional group. This compound typically exhibits a yellow to orange color due to the presence of the nitro group, which can also influence its reactivity and solubility. It is generally soluble in organic solvents such as dichloromethane and ethyl acetate, while being less soluble in water. The presence of the tert-butyl group enhances its stability and steric hindrance, making it less reactive compared to other carboxylate esters. This compound is often utilized in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, the nitro group can serve as a handle for further functionalization, allowing for the synthesis of more complex molecules. Safety data should be consulted for handling and storage, as nitro compounds can be sensitive to heat and shock.

tert-butyl 6-nitroindoline-1-carboxylate

129487-99-6: Tert-butyl 6-nitroindoline-1-carboxylate is an organic compound characterized by its indoline structure, which features a nitro group and a tert-butyl ester functional group. This compound typically exhibits a yellow to orange color due to the presence of the nitro group, which can also influence its reactivity and solubility. It is generally soluble in organic solvents such as dichloromethane and ethyl acetate, while being less soluble in water. The presence of the tert-butyl group enhances its stability and steric hindrance, making it less reactive compared to other carboxylate esters. This compound is often utilized in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, the nitro group can serve as a handle for further functionalization, allowing for the synthesis of more complex molecules. Safety data should be consulted for handling and storage, as nitro compounds can be sensitive to heat and shock.

CAS 129487-99-6

tert-butyl 6-nitroindoline-1-carboxylate

tert-Butyl 6-nitro-2,3-dihydroindole-1-carboxylate

Ref: IN-DA000Z6F

tert-Butyl 6-nitroindoline-1-carboxylate

Ref: 54-OR84362

TERT-BUTYL 6-NITROINDOLINE-1-CARBOXYLATE

Ref: 10-F387570