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CAS 850568-51-3

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[1-(tert-butoxycarbonyl)-6-methyl-1H-indol-2-yl]boronic acid

Description:
[1-(tert-butoxycarbonyl)-6-methyl-1H-indol-2-yl]boronic acid is a boronic acid derivative characterized by its unique structural features, which include an indole moiety substituted with a tert-butoxycarbonyl (Boc) group and a methyl group. 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 organic synthesis applications, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. The presence of the Boc group provides protection for the amine functionality, allowing for selective reactions under specific conditions. Additionally, the indole structure contributes to the compound's potential biological activity, as indoles are known for their presence in many natural products and pharmaceuticals. The compound is likely to be a solid at room temperature and may exhibit moderate solubility in organic solvents. Its reactivity and stability can be influenced by factors such as pH and the presence of other functional groups in a reaction mixture.
Formula:C14H18BNO4
InChI:InChI=1/C14H18BNO4/c1-9-5-6-10-8-12(15(18)19)16(11(10)7-9)13(17)20-14(2,3)4/h5-8,18-19H,1-4H3
SMILES:Cc1ccc2cc(B(O)O)n(c2c1)C(=O)OC(C)(C)C
Synonyms:
  • (1-(tert-Butoxycarbonyl)-6-methyl-1H-indol-2-yl)boronicacid
  • [1-(tert-Butoxycarbonyl)-6-methyl-1H-indol-2-yl]boronic acid
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