4-Bromo-1-(tert-butoxycarbonyl)-1H-indole-3-carboxylic acid is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of a bromine atom at the 4-position of the indole ring introduces a halogen substituent, which can influence the compound's reactivity and properties. The tert-butoxycarbonyl (Boc) group is a common protecting group in organic synthesis, particularly for amines, and it enhances the compound's stability and solubility. The carboxylic acid functional group at the 3-position contributes to the compound's acidity and potential for forming salts or esters. This compound is often utilized in synthetic organic chemistry, particularly in the synthesis of more complex molecules, due to its functional groups that allow for further chemical modifications. Its CAS number, 110811-31-9, uniquely identifies it in chemical databases, facilitating research and application in various fields, including pharmaceuticals and materials science.

4-BROMO-1-(TERT-BUTOXYCARBONYL)-1H-INDOLE-3-CARBOXYLIC ACID

110811-31-9: 4-Bromoindole-3-carboxylic acid, 4-Bromo-1H-Indole-3-Carboxylic Acid, 4-Bromoindole-3-carboxylic acid 97%

CAS 110811-31-9: 4-BROMO-1-(TERT-BUTOXYCARBONYL)-1H-INDOLE-3-CARBOXYLIC ACID

4-Bromo-1H-indole-3-carboxylic acid

Ref: 3D-KEA81131

4-Bromo-1H-indole-3-carboxylic acid

Ref: 10-F460574

4-Bromo-1H-indole-3-carboxylic acid

Ref: 54-OR12448

1H-Indole-3-carboxylicacid, 4-bromo-

Ref: IN-DA007C2Y