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CAS 136083-57-3

:

Fmoc-D-Asp-OH

Description:
Fmoc-D-Asp-OH, or Fluorenylmethyloxycarbonyl-D-aspartic acid, is a protected form of the amino acid aspartic acid, commonly used in peptide synthesis. The Fmoc group serves as a protective group for the amino functionality, allowing for selective reactions at the carboxylic acid site during peptide assembly. This compound is characterized by its stability under basic conditions, which facilitates its use in solid-phase peptide synthesis. Fmoc-D-Asp-OH is typically a white to off-white powder and is soluble in organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), but less soluble in water. Its molecular structure includes a fluorene ring, which contributes to its unique properties, including its ability to absorb UV light, making it useful for monitoring reactions. The presence of the D-configuration of aspartic acid imparts specific stereochemical properties, influencing the overall conformation of peptides synthesized with this amino acid. Overall, Fmoc-D-Asp-OH is a valuable reagent in the field of peptide chemistry and biochemistry.
Formula:C19H17NO6
Synonyms:
  • Fmoc-D-Aspartic Acid
  • N-Fmoc-D-Aspartic Acid
  • N-(9-Fluorenylmethoxycarbonyl)-D-Aspartic Acid
  • N-[(9H-Fluoren-9-Ylmethoxy)Carbonyl]-D-Aspartic Acid
  • N-Alpha-(9-Fluorenylmethoxycarbonyl)-D-Asparatic Acid
  • FMOC-D-ASP-OH
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