The chemical substance known as [1-tert-butoxycarbonyl-4-(3-hydroxy-3-methyl-butyl)-6-[[methyl(1,2,2-trimethylpropyl)amino]methyl]indol-2-yl]boronic acid, with the CAS number 943637-14-7, is a complex organic compound featuring a boronic acid functional group. This compound is characterized by its intricate molecular structure, which includes an indole core, a tert-butoxycarbonyl (Boc) protecting group, and a branched alkyl chain. The presence of the boronic acid moiety suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Additionally, the compound's structure indicates it may exhibit unique solubility and reactivity properties, influenced by the steric and electronic effects of the substituents. Its synthesis and characterization would typically involve advanced organic chemistry techniques, and it may serve as a valuable intermediate in the synthesis of more complex molecules or as a tool in chemical biology research. As with many boronic acids, it may also participate in reversible covalent bonding with diols, which is significant in various biochemical applications.

[1-tert-butoxycarbonyl-4-(3-hydroxy-3-methyl-butyl)-6-[[methyl(1,2,2-trimethylpropyl)amino]methyl]indol-2-yl]boronic acid

943637-14-7: The chemical substance known as [1-tert-butoxycarbonyl-4-(3-hydroxy-3-methyl-butyl)-6-[[methyl(1,2,2-trimethylpropyl)amino]methyl]indol-2-yl]boronic acid, with the CAS number 943637-14-7, is a complex organic compound featuring a boronic acid functional group. This compound is characterized by its intricate molecular structure, which includes an indole core, a tert-butoxycarbonyl (Boc) protecting group, and a branched alkyl chain. The presence of the boronic acid moiety suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Additionally, the compound's structure indicates it may exhibit unique solubility and reactivity properties, influenced by the steric and electronic effects of the substituents. Its synthesis and characterization would typically involve advanced organic chemistry techniques, and it may serve as a valuable intermediate in the synthesis of more complex molecules or as a tool in chemical biology research. As with many boronic acids, it may also participate in reversible covalent bonding with diols, which is significant in various biochemical applications.

CAS 943637-14-7

[1-tert-butoxycarbonyl-4-(3-hydroxy-3-methyl-butyl)-6-[[methyl(1,2,2-trimethylpropyl)amino]methyl]indol-2-yl]boronic acid

2-BORONO-4-(3-HYDROXY-3-METHYLBUTYL)-6-[[METHYL(1,2,2-TRIMETHYLPROPYL)AMINO]METHYL]-1H-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

Ref: IN-DA00II39