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CAS 850568-43-3

:

(2-{[(tert-butoxycarbonyl)amino]methyl}-5-fluorophenyl)boronic acid

Description:
(2-{[(tert-butoxycarbonyl)amino]methyl}-5-fluorophenyl)boronic acid is a boronic acid derivative characterized by its unique functional groups, which include a boronic acid moiety, an amino group protected by a tert-butoxycarbonyl (Boc) group, and a fluorinated phenyl ring. 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 fluorine atom can enhance the compound's lipophilicity and influence its biological activity. The Boc group serves as a protective group, allowing for selective reactions without interfering with the amino functionality. Additionally, the compound's structure suggests potential for use in drug development, particularly in the design of inhibitors targeting specific enzymes or receptors. Its solubility and stability in various solvents can vary, depending on the pH and the presence of other functional groups. Overall, this compound represents a versatile building block in the synthesis of more complex molecules.
Formula:C12H17BFNO4
InChI:InChI=1/C12H17BFNO4/c1-12(2,3)19-11(16)15-7-8-4-5-9(14)6-10(8)13(17)18/h4-6,17-18H,7H2,1-3H3,(H,15,16)
SMILES:CC(C)(C)OC(=NCc1ccc(cc1B(O)O)F)O
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