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CAS 2121513-97-9

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B-[3-(Aminocarbonyl)-5-bromophenyl]boronic acid

Description:
B-[3-(Aminocarbonyl)-5-bromophenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and is widely used in organic synthesis and medicinal chemistry. The compound features a bromophenyl moiety, which contributes to its electronic properties and potential reactivity. The aminocarbonyl group enhances its solubility and may influence its biological activity, making it a candidate for applications in drug development or as a building block in the synthesis of more complex molecules. The presence of both the boronic acid and the aminocarbonyl functionalities suggests potential utility in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. Additionally, the compound's structure may allow for interactions with biological targets, making it of interest in the field of pharmaceuticals. Overall, B-[3-(Aminocarbonyl)-5-bromophenyl]boronic acid exemplifies the versatility of boronic acids in synthetic and medicinal chemistry.
Formula:C7H7BBrNO3
InChI:InChI=1S/C7H7BBrNO3/c9-6-2-4(7(10)11)1-5(3-6)8(12)13/h1-3,12-13H,(H2,10,11)
InChI key:InChIKey=VUEQXFIUMDEIIM-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C(N)=O)=CC(Br)=C1
Synonyms:
  • Boronic acid, B-[3-(aminocarbonyl)-5-bromophenyl]-
  • B-[3-(Aminocarbonyl)-5-bromophenyl]boronic acid
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