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CAS 1231709-22-0

:

FMoc-(R)-2-aMino-2-Methylbutanoic acid

Description:
FMoc-(R)-2-Amino-2-methylbutanoic acid is a protected amino acid commonly used in peptide synthesis. The "FMoc" (9-fluorenylmethoxycarbonyl) group serves as a temporary protective group for the amino function, allowing for selective reactions without interfering with other functional groups. This compound features a chiral center, which contributes to its stereochemical properties, making it valuable in the synthesis of enantiomerically pure peptides. The presence of the methyl group on the alpha carbon enhances its hydrophobic characteristics, influencing solubility and reactivity in various solvents. Additionally, the carboxylic acid functional group allows for the formation of peptide bonds, facilitating its incorporation into larger peptide chains. The compound is typically handled under standard laboratory conditions, and its stability can be affected by factors such as pH and temperature. Overall, FMoc-(R)-2-amino-2-methylbutanoic acid is an important building block in the field of medicinal chemistry and biochemistry, particularly in the development of pharmaceuticals and biologically active compounds.
Formula:C20H21NO4
Synonyms:
  • (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2-methylbutanoic acid
  • Fmoc-α-Me-D-Gly(Ethyl)-OH
  • FMoc-(R)-2-aMino-2-Methylbutanoic acid
  • FMoc-α-Me-D-Gly(Ethyl)-OH
  • (R)-N-FMOC-Α-ETHYLALANINE
  • D-Isovaline, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
  • (9H-Fluoren-9-yl)MethOxy]Carbonyl D-IsoValine
  • N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-isovaline
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