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Catalog Number:
02417
CAS Number:
86060-85-7
Éster pentafluorofenilo de Fmoc-glicina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-Gly-OPfp
Documents
$27.94 /1G
Tamaño
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Información del producto

Fmoc-glycine pentafluorophenyl ester is a highly versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique pentafluorophenyl group, which enhances its reactivity and stability, making it an ideal choice for researchers focused on developing complex peptide structures. The Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of peptides with high purity and yield. Its application extends to the pharmaceutical industry, where it plays a crucial role in the design of novel therapeutics, particularly in the development of peptide-based drugs.

Researchers appreciate the compound's ability to streamline the synthesis process while maintaining the integrity of sensitive functional groups. The pentafluorophenyl ester moiety not only improves solubility but also enhances the overall efficiency of coupling reactions. This makes Fmoc-glycine pentafluorophenyl ester a preferred choice for professionals aiming to optimize their peptide synthesis workflows, ensuring high-quality results in various applications, from academic research to industrial production.

Número CAS
86060-85-7
Fórmula molecular
C23H14F5NO4
Peso molecular
463.4
Número MDL
MFCD00037641
Punto de fusión
155 - 160 ºC
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
86060-85-7
Fórmula molecular
C23H14F5NO4
Peso molecular
463.4
Número MDL
MFCD00037641
Punto de fusión
155 - 160 ºC
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-glycine pentafluorophenyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the introduction of glycine residues with enhanced stability and reactivity.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, particularly in creating compounds with improved bioavailability.
  • Bioconjugation: The chemical is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other compounds, which is essential in diagnostics and therapeutic applications.
  • Research in Protein Engineering: Researchers utilize this ester in studies aimed at modifying protein structures, which can lead to advancements in enzyme activity and specificity.
  • Fluorinated Compound Research: Its pentafluorophenyl group allows for the exploration of fluorinated compounds, which can exhibit unique properties beneficial in materials science and chemical reactions.