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CAS 1072945-73-3

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B-[3-[(Cyclohexylmethylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-[(Cyclohexylmethylamino)carbonyl]phenyl]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, making it useful in various applications, including medicinal chemistry and materials science. The compound features a phenyl ring substituted with a cyclohexylmethylamino group, which enhances its solubility and biological activity. The boronic acid moiety contributes to its reactivity, particularly in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the cyclohexylmethylamino group may impart specific pharmacological properties, potentially influencing its interaction with biological targets. This compound is of interest in the development of therapeutic agents, especially in the context of cancer research and drug design, due to its ability to modulate biological pathways. Overall, B-[3-[(Cyclohexylmethylamino)carbonyl]phenyl]boronic acid exemplifies the versatility of boronic acids in both synthetic and biological chemistry.
Formula:C14H20BNO3
InChI:InChI=1S/C14H20BNO3/c1-16(13-8-3-2-4-9-13)14(17)11-6-5-7-12(10-11)15(18)19/h5-7,10,13,18-19H,2-4,8-9H2,1H3
InChI key:InChIKey=MFWBKTUXYRRWCS-UHFFFAOYSA-N
SMILES:C(N(C)C1CCCCC1)(=O)C2=CC(B(O)O)=CC=C2
Synonyms:
  • B-[3-[(Cyclohexylmethylamino)carbonyl]phenyl]boronic acid
  • [3-[Cyclohexyl(methyl)carbamoyl]phenyl]boronic acid
  • Boronic acid, B-[3-[(cyclohexylmethylamino)carbonyl]phenyl]-
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