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CAS 913388-66-6

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[1-tert-butoxycarbonyl-5-(tert-butoxycarbonylamino)indol-2-yl]boronic acid

Description:
[1-tert-butoxycarbonyl-5-(tert-butoxycarbonylamino)indol-2-yl]boronic acid is a boronic acid derivative characterized by the presence of both boron and indole functional groups. This compound features a boronic acid moiety, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The tert-butoxycarbonyl (Boc) groups provide protection for the amino functionalities, enhancing the compound's stability and facilitating its use in peptide synthesis. The indole structure contributes to the compound's potential biological activity, as indoles are often found in pharmaceuticals and natural products. Additionally, the presence of the boronic acid group may impart unique reactivity, allowing for participation in cross-coupling reactions. Overall, this compound exemplifies the intersection of organic synthesis and medicinal chemistry, showcasing the versatility of boronic acids in functionalizing complex molecular architectures.
Formula:C18H25BN2O6
InChI:InChI=1/C18H25BN2O6/c1-17(2,3)26-15(22)20-12-7-8-13-11(9-12)10-14(19(24)25)21(13)16(23)27-18(4,5)6/h7-10,24-25H,1-6H3,(H,20,22)
SMILES:CC(C)(C)OC(=O)Nc1ccc2c(c1)cc(B(O)O)n2C(=O)OC(C)(C)C
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