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CAS 850567-25-8

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

Description:
B-[3-[(Cyclohexylamino)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 organic synthesis and medicinal chemistry. This compound features a phenyl ring substituted with a cyclohexylamino carbonyl group, contributing to its structural complexity and potential biological activity. The boronic acid moiety allows for participation in Suzuki coupling reactions, a key method in the formation of carbon-carbon bonds. Additionally, the cyclohexylamino group may enhance solubility and influence the compound's interaction with biological targets. The compound's properties, such as solubility, stability, and reactivity, can be influenced by the presence of the boron atom and the substituents on the phenyl ring. Overall, B-[3-[(Cyclohexylamino)carbonyl]phenyl]boronic acid represents a versatile building block in synthetic chemistry and has potential applications in drug development and materials science.
Formula:C13H18BNO3
InChI:InChI=1S/C13H18BNO3/c16-13(15-12-7-2-1-3-8-12)10-5-4-6-11(9-10)14(17)18/h4-6,9,12,17-18H,1-3,7-8H2,(H,15,16)
InChI key:InChIKey=PZOTXXRWCKDMBC-UHFFFAOYSA-N
SMILES:C(NC1CCCCC1)(=O)C2=CC(B(O)O)=CC=C2
Synonyms:
  • 3-(Cyclohexylcarbamoyl)phenylboronic acid
  • B-[3-[(Cyclohexylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, [3-[(cyclohexylamino)carbonyl]phenyl]-
  • Boronicacid, [3-[(cyclohexylamino)carbonyl]phenyl]- (9CI)
  • Boronic acid, B-[3-[(cyclohexylamino)carbonyl]phenyl]-
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