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Catalog Number:
05677
CAS Number:
86061-03-2
Éster β-bencílico del ácido Fmoc-L-aspártico y éster α-pentafluorofenílico
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-L-Asp(OBzl)-OPfp
Documents
$180.00 /1G
Tamaño
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Información del producto

Fmoc-L-aspartic acid b-benzyl ester a-pentafluorophenyl ester is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique structure that enhances its reactivity and stability, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides with high purity and yield. The presence of the pentafluorophenyl ester moiety further enhances its lipophilicity, which can improve the bioavailability of the resulting peptides.

This compound is particularly valuable in the synthesis of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its ability to form stable intermediates makes it a preferred choice for researchers looking to streamline their synthesis processes. Additionally, the benzyl ester group provides a convenient handle for further functionalization, allowing for the development of novel compounds with tailored properties. Overall, Fmoc-L-aspartic acid b-benzyl ester a-pentafluorophenyl ester stands out as a powerful tool for advancing peptide chemistry and drug discovery.

Número CAS
86061-03-2
Fórmula molecular
C32H22NO6F5
Peso molecular
611.53
Número MDL
MFCD00237044
Punto de fusión
138 - 141 °C
Rotación óptica
[a] D 20 = -24 ± 1 ° (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
86061-03-2
Fórmula molecular
C32H22NO6F5
Peso molecular
611.53
Número MDL
MFCD00237044
Punto de fusión
138 - 141 °C
Rotación óptica
[a] D 20 = -24 ± 1 ° (C=1 en DMF)
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

Fmoc-L-aspartic acid b-benzyl ester a-pentafluorophenyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), enhancing the efficiency and yield of the process.
  • Drug Development: It plays a significant role in the pharmaceutical industry for developing new drugs, especially those targeting neurological disorders, by facilitating the modification of peptide structures.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in creating targeted therapies and diagnostics.
  • Research in Protein Engineering: It aids in the design of modified proteins with enhanced properties, making it valuable in biotechnology and enzyme engineering applications.
  • Fluorinated Compound Applications: The presence of pentafluorophenyl groups provides unique properties, such as increased stability and lipophilicity, making it beneficial in materials science and the development of advanced functional materials.

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