1-BOC-5-amino-2,3-dihydro-indole, with the CAS number 129487-92-9, is a chemical compound characterized by its bicyclic structure, which includes an indole moiety. The "1-BOC" designation indicates the presence of a tert-butyloxycarbonyl (BOC) protecting group on the nitrogen atom at the first position of the indole ring. This protecting group is commonly used in organic synthesis to temporarily mask amine functionalities, facilitating various chemical reactions without interference from the amine. The compound features an amino group at the fifth position of the indole, contributing to its reactivity and potential applications in medicinal chemistry. It is typically a white to off-white solid and is soluble in organic solvents. The presence of the dihydro form suggests that it has undergone partial hydrogenation, which can influence its biological activity and stability. Overall, 1-BOC-5-amino-2,3-dihydro-indole is of interest in the synthesis of pharmaceuticals and other bioactive compounds due to its structural features and functional groups.

1-BOC-5-AMINO-2,3-DIHYDRO-INDOLE

129487-92-9: 5-Amino-1-Boc-2,3-Dihydroindole, 5-Amino-2,3-Dihydro-Indole-1-Carboxylic Acid Tert-Butyl Ester, 1H-Indole-1-carboxylic acid, 5-amino-2,3-dihydro-, 1,1-dimethylethyl ester

tert-Butyl 5-amino-2,3-dihydro-1H-indole-1-carboxylate

CAS 129487-92-9: 1-BOC-5-AMINO-2,3-DIHYDRO-INDOLE

tert-Butyl 5-amino-2,3-dihydro-1H-indole-1-carboxylate

Ref: 54-OR305256

Tert-Butyl 5-aminoindoline-1-carboxylate

Ref: 10-F225662

1H-Indole-1-carboxylic acid, 5-amino-2,3-dihydro-, 1,1-dimethylethyl ester

Ref: IN-DA000Z6G

5-Amino-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester

Ref: 3D-EFA48792