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CAS 204384-69-0

:

Benzenebutanoic acid,4-(1,1-dimethylethoxy)-a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (aS)-

Description:
Benzenebutanoic acid, 4-(1,1-dimethylethoxy)-α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αS)-, is a complex organic compound characterized by its multi-functional structure. It features a benzenebutanoic acid backbone, which contributes to its acidic properties, and a 1,1-dimethylethoxy group that enhances its steric bulk and solubility characteristics. The presence of the fluorenylmethoxycarbonyl (Fmoc) group indicates its use in peptide synthesis, particularly as a protective group for amino acids. This compound is likely to exhibit moderate to high lipophilicity due to its aromatic and aliphatic components, influencing its interactions in biological systems. Additionally, the stereochemistry indicated by (αS)- suggests specific spatial arrangements that may affect its reactivity and biological activity. Overall, this compound is of interest in medicinal chemistry and biochemistry, particularly in the development of pharmaceuticals and peptide-based therapeutics. Its unique structure allows for diverse applications, including drug design and synthesis methodologies.
Formula:C29H31NO5
Synonyms:
  • Benzenebutanoicacid, 4-(1,1-dimethylethoxy)-a-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (S)-
  • (S)-2-(Fmoc-amino)-4-(4-tert-butoxyphenyl)butanoic acid
  • Benzenebutanoic acid, 4-(1,1-dimethylethoxy)-α-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (αS)-
  • FMOC-L-HOMOPHENYL-ALA
  • fmoc-L-Homotyrosine(OtBu)-OH
  • FMOC-(S)-2-AMINO-4-PHENYLBUTYRIC ACID
  • (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-[4-(propan-2-yloxy)phenyl]butanoic acid
  • FMOC-L-HPHE
  • (S)-2-(9H-FLUOREN-9-YLMETHOXYCARBONYLAMINO)-4-PHENYL-BUTYRIC ACID
  • Fmoc-L-HTyr(tBu)-OH USP/EP/BP
  • See more synonyms
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