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Catalog Number:
04973
CAS Number:
188970-92-5
Ácido N a -Fmoc-N b -aliloxicarbonil-L-2,3-diaminopropiónico
Purity:
≥ 95 % (HPLC)
Synonym(s):
Fmoc-L-Dap(Aloc)-OH
Documents
$48.67 /250 mg
Tamaño
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Información del producto

Na-Fmoc-Nb-allyloxycarbonyl-L-2,3-diaminopropionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a protective Fmoc group, which is crucial for the selective deprotection of amines during solid-phase peptide synthesis. Its unique allyloxycarbonyl group enhances its reactivity and stability, making it an excellent choice for researchers looking to create complex peptide structures with precision. The compound's ability to facilitate the incorporation of non-standard amino acids into peptides opens up new avenues in the design of therapeutic peptides and biologically active compounds.

In addition to its applications in peptide synthesis, Na-Fmoc-Nb-allyloxycarbonyl-L-2,3-diaminopropionic acid is also valuable in the development of novel drug candidates and biomaterials. Its structural features allow for the modification of peptide sequences, which can lead to improved pharmacological properties and targeted delivery systems. Researchers and industry professionals can leverage this compound to enhance their projects in drug discovery, biomolecular engineering, and therapeutic development, making it a vital addition to any chemical toolkit.

Número CAS
188970-92-5
Fórmula molecular
C22H22N2O6
Peso molecular
410.53
Número MDL
MFCD00273468
Punto de fusión
140 - 160 °C
Rotación óptica
[a] D 20 = -21,5 ± 2 º (C=2 en DMF) D 20 = -10, ± 2º (C=1 en MeOH)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
188970-92-5
Fórmula molecular
C22H22N2O6
Peso molecular
410.53
Número MDL
MFCD00273468
Punto de fusión
140 - 160 °C
Rotación óptica
[a] D 20 = -21,5 ± 2 º (C=2 en DMF) D 20 = -10, ± 2º (C=1 en MeOH)
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
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Aplicaciones

Na-Fmoc-Nb-allyloxycarbonyl-L-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting the overall structure. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: It plays a significant role in the design of new drug candidates, particularly in creating compounds that can target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Biochemistry: It is valuable in biochemical research for studying protein interactions and functions, aiding scientists in understanding cellular mechanisms and disease pathways.
  • Material Science: The compound finds applications in the development of functional materials, such as hydrogels, which can be used in tissue engineering and regenerative medicine.

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