CAS 1310384-28-1
:1-Boc-5,6-dichloro-1H-indole-2-boronicacid
Description:
1-Boc-5,6-dichloro-1H-indole-2-boronic 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 "Boc" (tert-butyloxycarbonyl) group is a common protecting group used in organic synthesis, particularly in the protection of amines. The presence of dichloro substituents at the 5 and 6 positions of the indole ring indicates that this compound has enhanced reactivity and potential for further functionalization. The boronic acid functionality is significant for its ability to form covalent bonds with diols and is widely utilized in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. This compound may be of interest in medicinal chemistry and materials science due to its unique structural features and potential applications in drug development and organic synthesis. Its specific properties, such as solubility, stability, and reactivity, would depend on the surrounding conditions and the presence of other functional groups.
Formula:C13H14BCl2NO4
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Found 3 products.
1-Boc-5,6-dichloro-1h-indole-2-boronic acid
CAS:Formula:C13H14BCl2NO4Purity:95%Color and Shape:SolidMolecular weight:329.9716(1-(tert-Butoxycarbonyl)-5,6-dichloro-1H-indol-2-yl)boronic acid
CAS:(1-(tert-Butoxycarbonyl)-5,6-dichloro-1H-indol-2-yl)boronic acidPurity:95%Molecular weight:329.97g/mol1-Boc-5,6-Dichloro-1H-indole-2-boronic acid
CAS:Formula:C13H14BCl2NO4Purity:95%Molecular weight:329.97


