5-Bromo-1-(triisopropylsilyl)-1H-indole is a chemical compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a bromine atom at the 5-position of the indole ring introduces a halogen substituent, which can influence the compound's reactivity and potential applications in organic synthesis. The triisopropylsilyl group serves as a protecting group for the nitrogen atom in the indole, enhancing the compound's stability and solubility in organic solvents. This compound is typically used in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to undergo various chemical transformations. Its unique structural features allow for selective reactions, making it a valuable intermediate in the synthesis of more complex molecules. Additionally, the presence of the silyl group can facilitate purification processes and improve yields in subsequent reactions. Overall, 5-bromo-1-(triisopropylsilyl)-1H-indole is a versatile compound with significant utility in chemical research and development.

5-BROMO-1-(TRIISOPROPYLSILYL)-1H-INDOLE

128564-66-9: 5-bromo-1-[tris(1-methylethyl)silyl]-1H-indole, 5-bromo-1-(triisopropylsilyl)-1H-indole

5-Bromo-1-(triisopropylsilyl)-1h-indole is a natural alkaloid. It is the first example of an efficient, enantioselective synthesis of diketopiperazine. The key step in this synthesis is the regioselective, stereoselective dihydroxylation of 5-bromoindole with sodium hypochlorite as the oxidant and tertiary butanol as a solvent. This reaction results in the formation of two products: 5-bromo-1-(triisopropylsilyl)-1h-indole and 1-(2,2,2-trimethylpropoxy)butane.

CAS 128564-66-9: 5-BROMO-1-(TRIISOPROPYLSILYL)-1H-INDOLE

5-Bromo-1-(triisopropylsilyl)-1h-indole

Ref: 3D-FB154472

5-BROMO-1-(TRIISOPROPYLSILYL)-1H-INDOLE

Ref: 10-F501801

1H-Indole, 5-bromo-1-[tris(1-methylethyl)silyl]-

Ref: IN-DA000Y7U