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CAS 848357-46-0

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(1-tert-butoxycarbonyl-6-methoxycarbonyl-indol-2-yl)boronic acid

Description:
(1-tert-butoxycarbonyl-6-methoxycarbonyl-indol-2-yl)boronic acid is a boronic acid derivative characterized by its unique structural features, which include an indole core substituted with both tert-butoxycarbonyl and methoxycarbonyl groups. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the indole moiety contributes to its potential biological activity, as indole derivatives are often found in pharmaceuticals. Additionally, the tert-butoxycarbonyl (Boc) group serves as a protective group in organic synthesis, allowing for selective reactions. The compound is likely to be a solid at room temperature and may have moderate solubility in organic solvents. Its reactivity and stability can be influenced by the presence of functional groups, making it a versatile intermediate in the synthesis of more complex molecules. Overall, this compound exemplifies the intersection of organic chemistry and medicinal applications, highlighting the importance of boronic acids in contemporary research.
Formula:C15H18BNO6
InChI:InChI=1/C15H18BNO6/c1-15(2,3)23-14(19)17-11-7-10(13(18)22-4)6-5-9(11)8-12(17)16(20)21/h5-8,20-21H,1-4H3
SMILES:CC(C)(C)OC(=O)n1c2cc(ccc2cc1B(O)O)C(=O)OC
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