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CAS 871332-87-5

:

[3-(tert-butylcarbamoyl)-5-nitro-phenyl]boronic acid

Description:
[3-(tert-butylcarbamoyl)-5-nitro-phenyl]boronic acid is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl ring that is substituted with a nitro group and a tert-butylcarbamoyl 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 applications including organic synthesis and medicinal chemistry. The presence of the nitro group often enhances the compound's reactivity and polarity, while the tert-butylcarbamoyl group can influence solubility and stability. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds in organic synthesis. The compound's structure suggests potential applications in drug development and materials science, particularly in the design of targeted therapies or as intermediates in the synthesis of more complex molecules. Overall, its unique functional groups contribute to its chemical behavior and potential utility in various chemical processes.
Formula:C11H15BN2O5
InChI:InChI=1/C11H15BN2O5/c1-11(2,3)13-10(15)7-4-8(12(16)17)6-9(5-7)14(18)19/h4-6,16-17H,1-3H3,(H,13,15)
SMILES:CC(C)(C)N=C(c1cc(cc(c1)N(=O)=O)B(O)O)O
Synonyms:
  • [3-(tert-Butylcarbamoyl)-5-nitrophenyl]boronic acid
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