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CAS 192804-36-7

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(4-Cbz-aminophenyl)boronic acid

Description:
(4-Cbz-aminophenyl)boronic acid, with the CAS number 192804-36-7, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a carbobenzyloxy (Cbz) group. This compound typically exhibits properties such as being a white to off-white solid, soluble in organic solvents like methanol and dichloromethane, and showing limited solubility in water due to its hydrophobic Cbz group. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. The Cbz group serves as a protecting group for amines, facilitating the selective functionalization of the amine without interference from other reactive sites. Additionally, (4-Cbz-aminophenyl)boronic acid can exhibit interesting biological activities, which may be explored in drug development and materials science. Its stability and reactivity are influenced by factors such as pH and the presence of other functional groups in a reaction environment.
Formula:C14H14BNO4
InChI:InChI=1/C14H14BNO4/c17-14(20-10-11-4-2-1-3-5-11)16-13-8-6-12(7-9-13)15(18)19/h1-9,18-19H,10H2,(H,16,17)
SMILES:c1ccc(cc1)COC(=O)Nc1ccc(cc1)B(O)O
Synonyms:
  • [4-[(Benzyloxycarbonylamino)phenyl]boronic acid
  • (4-{[(Benzyloxy)Carbonyl]Amino}Phenyl)Boronic Acid
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