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CAS 475102-13-7

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1-N-Boc-5-bromoindole-2-boronic acid

Description:
1-N-Boc-5-bromoindole-2-boronic acid is a chemical compound that belongs to the class of boronic acids and indole derivatives. It features a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in Suzuki coupling reactions. The presence of the Boc (tert-butyloxycarbonyl) protecting group enhances its stability and solubility, while the bromine atom at the 5-position of the indole ring provides a site for further functionalization. This compound is typically used in medicinal chemistry and material science for the development of biologically active molecules and polymers. Its unique structure allows for potential applications in drug discovery, particularly in targeting specific biological pathways. The compound is generally handled with standard laboratory safety precautions, as with other boronic acids, due to potential reactivity and toxicity.
Formula:C13H15BBrNO4
InChI:InChI=1/C13H15BBrNO4/c1-13(2,3)20-12(17)16-10-5-4-9(15)6-8(10)7-11(16)14(18)19/h4-7,18-19H,1-3H3
SMILES:CC(C)(C)OC(=O)n1c2ccc(cc2cc1B(O)O)Br
Synonyms:
  • [5-Bromo-1-(tert-butoxycarbonyl)-1H-indol-2-yl]boronic acid
  • 1H-Indole-1-carboxylic acid, 2-borono-5-bromo-, 1,1-dimethylethyl ester
  • 5-Bromo-1-(tert-butoxycarbonyl)-1H-indol-2-ylboronic acid
  • N-Boc-5-bromoindole-2-boronic acid
  • T56 Bnj Bvox1&1&1 Cbqq Ge [Wln]
  • 5-Bromo-1-T-Butoxycarbonylindole-2-Boronic Acid
  • N-(TERT-BUTOXYCARBONYL)5-BROMO-1H-INDOLE-2-BORONIC ACID
  • 1-BOC-5-BROMOINDOLE-2-BORONIC ACID
  • 1-BOC-5-BROMO-1H-INDOLE-2-BORONIC ACID
  • 5-Bromo-1H-indole-2-boronic acid, N-BOC protected
  • See more synonyms
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