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CAS 142121-93-5

:

4-FLUOROPHENYLGLYCINE-N-BOC PROTECTED

Description:
4-Fluorophenylglycine-N-Boc protected, with the CAS number 142121-93-5, is an organic compound characterized by the presence of a fluorine atom on the phenyl ring and a Boc (tert-butyloxycarbonyl) protecting group on the amine functional group. This compound is typically used in organic synthesis, particularly in the preparation of peptides and other biologically active molecules. The Boc group serves to protect the amine during various chemical reactions, allowing for selective modifications of other functional groups. The fluorine substitution can influence the compound's electronic properties and steric effects, potentially enhancing its biological activity or altering its interaction with biological targets. In terms of physical properties, it is likely to be a solid at room temperature, with solubility in organic solvents. The compound's stability, reactivity, and potential applications in medicinal chemistry make it of interest in research and development within pharmaceutical sciences. Proper handling and storage conditions are essential due to the potential reactivity of the functional groups involved.
Formula:C13H16FNO4
InChI:InChI=1/C13H16FNO4/c1-13(2,3)19-12(18)15-10(11(16)17)8-4-6-9(14)7-5-8/h4-7,10H,1-3H3,(H,15,18)(H,16,17)
SMILES:CC(C)(C)OC(=NC(c1ccc(cc1)F)C(=O)O)O
Synonyms:
  • N-Boc- 4-Fluorophenylglycine
  • [(Tert-Butoxycarbonyl)Amino](4-Fluorophenyl)Acetic Acid
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