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CAS 1926137-46-3

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1-[(tert-Butoxy)carbonyl]-3,4-dihydro-2H-quinoline-7-yboronic acid

Description:
1-[(tert-Butoxy)carbonyl]-3,4-dihydro-2H-quinoline-7-boronic acid is a chemical compound characterized by its unique structure, which includes a quinoline core, a boronic acid functional group, and a tert-butoxycarbonyl (Boc) protecting group. The presence of the boronic acid moiety suggests potential applications in organic synthesis, particularly in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds. The tert-butoxycarbonyl group serves as a protective group for amines, facilitating the selective functionalization of the compound. This compound is likely to be a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its reactivity can be influenced by the boronic acid group, which can participate in various chemical transformations. Additionally, the quinoline structure may impart specific biological activities, making it of interest in medicinal chemistry. Overall, this compound represents a versatile building block in synthetic organic chemistry, with potential applications in drug development and material science.
Formula:C14H20BNO4
Synonyms:
  • 1-BOC-1,2,3,4-Tetrahydroquinoline-7-boronic acid
  • 1-[(tert-Butoxy)carbonyl]-3,4-dihydro-2H-quinoline-7-yboronic acid
  • (1-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroquinolin-7-yl)boronic acid
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