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CAS 77119-85-8

:

(R)-(+)-2-(tert-butoxycarbonylamino)-3-phenylprop

Description:
(R)-(+)-2-(tert-butoxycarbonylamino)-3-phenylpropanoic acid, commonly referred to by its CAS number 77119-85-8, is an amino acid derivative characterized by its chiral center, which contributes to its enantiomeric properties. This compound features a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines during chemical reactions. The presence of a phenyl group on the propanoic acid backbone enhances its hydrophobic characteristics, influencing its solubility and reactivity. The (R)-enantiomer indicates a specific spatial arrangement of atoms, which can significantly affect the compound's biological activity and interactions with other molecules. This compound is often utilized in peptide synthesis and pharmaceutical applications due to its ability to serve as a building block for more complex structures. Its stability and reactivity can be influenced by factors such as pH and temperature, making it important to consider these conditions during handling and experimentation. Overall, this compound exemplifies the importance of chirality and functional group manipulation in organic chemistry.
Formula:C14H19NO3
Synonyms:
  • (R)-(+)-2-(tert-Butoxycarbonylamino)-3-phenylpropanal
  • N-t-BOC-D-phenylalaninal
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