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CAS 487027-89-4

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FMoc-L-2,3-diaMinopropionic acid hydrochloride

Description:
FMoc-L-2,3-diaminopropionic acid hydrochloride is a derivative of amino acids, specifically designed for use in peptide synthesis and research applications. It features a protected amino group, with the FMoc (9-fluorenylmethoxycarbonyl) group serving as a temporary protective group that facilitates the assembly of peptides by preventing unwanted reactions during synthesis. The compound contains two amino groups, which contribute to its potential for forming various peptide bonds and interactions. As a hydrochloride salt, it is typically more soluble in water, enhancing its utility in biological and chemical applications. The presence of the L-configuration indicates its relevance in biological systems, as L-amino acids are the building blocks of proteins. This compound is often utilized in the development of pharmaceuticals and in the study of peptide interactions due to its structural characteristics. Its stability, solubility, and reactivity make it a valuable tool in organic synthesis and biochemistry.
Formula:C18H19ClN2O4
Synonyms:
  • (2R)-3-amino-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanoic acid hydrochloride
  • (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)-amino)-3-aminopropanoic acid hydrochloride
  • N-α-(9-Fluorenylmethoxycarbonyl)-D-α,β-diaminopropionic acid hydrochloride
  • (S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-3-aMinopropanoic acid hydrochloride
  • (2R)-3-amino-2-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid
  • Fmoc-d-dap-oh hydrochloride
  • 3-Amino-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-D-alanine monohydrochloride
  • 3-Amino-N-Fmoc-D-alanine HCl
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