3,4-Difluoro-D-phenylalanine is a fluorinated derivative of the amino acid phenylalanine, characterized by the presence of two fluorine atoms at the 3 and 4 positions of the aromatic ring. This modification can significantly influence its biochemical properties, including its solubility, reactivity, and interaction with biological systems. The presence of fluorine atoms often enhances the compound's stability and can alter its pharmacokinetic properties, making it of interest in medicinal chemistry and drug design. As a D-enantiomer, it may exhibit different biological activities compared to its L-counterpart, which is the naturally occurring form. The compound is typically used in research settings, particularly in studies related to protein engineering and the development of novel therapeutics. Its unique structural features may also allow for specific interactions with enzymes or receptors, potentially leading to applications in targeted drug delivery or as a building block in the synthesis of more complex molecules. Safety and handling precautions should be observed due to the presence of fluorinated compounds, which can exhibit unique toxicological profiles.

3,4-difluoro-D-phenylalanine

249648-08-6: 3,4-Difluoro-D-phenylalanine is a fluorinated derivative of the amino acid phenylalanine, characterized by the presence of two fluorine atoms at the 3 and 4 positions of the aromatic ring. This modification can significantly influence its biochemical properties, including its solubility, reactivity, and interaction with biological systems. The presence of fluorine atoms often enhances the compound's stability and can alter its pharmacokinetic properties, making it of interest in medicinal chemistry and drug design. As a D-enantiomer, it may exhibit different biological activities compared to its L-counterpart, which is the naturally occurring form. The compound is typically used in research settings, particularly in studies related to protein engineering and the development of novel therapeutics. Its unique structural features may also allow for specific interactions with enzymes or receptors, potentially leading to applications in targeted drug delivery or as a building block in the synthesis of more complex molecules. Safety and handling precautions should be observed due to the presence of fluorinated compounds, which can exhibit unique toxicological profiles.

CAS 249648-08-6

3,4-difluoro-D-phenylalanine

D-Phenylalanine, 3,4-difluoro-

Ref: IN-DA002Q0H

3,4-Difluoro-D-phenylalanine

Ref: 54-PC8364

(R)-2-Amino-3-(3,4-difluorophenyl)propanoic acid

Ref: 10-F235605