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Catalog Number:
02718
CAS Number:
130309-37-4
Ácido fmoc-L-octahidroindol-2-carboxílico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Oic-OH, (2 S ,3a S ,7a S )-1-Fmoc-octahidro-1 H -indol-2-ácido carboxílico
Documents
$25.00 /250 mg
Tamaño
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Información del producto

Fmoc-L-octahydroindole-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a unique octahydroindole structure, which enhances its utility in the design of bioactive peptides and pharmaceuticals. The Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for selective deprotection during synthesis, making it an ideal choice for researchers focused on complex peptide sequences. Its application extends to the development of novel therapeutic agents, particularly in the fields of oncology and neurology, where such compounds can mimic natural biological processes.

Researchers appreciate Fmoc-L-octahydroindole-2-carboxylic acid for its stability and ease of use in various organic reactions. Its ability to facilitate the synthesis of cyclic peptides and other complex structures positions it as a valuable tool in medicinal chemistry. With its favorable properties, this compound not only streamlines the synthesis process but also enhances the overall yield and purity of the final products, making it a preferred choice among professionals in the pharmaceutical industry.

Número CAS
130309-37-4
Fórmula molecular
C24H25NO4
Peso molecular
391.5
Número MDL
MFCD09750487
Rotación óptica
[a] D 20 = -25 ± 3º (C=1 en DMF) D 20 = -38 ± 3º (C=1 en EtOH)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
130309-37-4
Fórmula molecular
C24H25NO4
Peso molecular
391.5
Número MDL
MFCD09750487
Rotación óptica
[a] D 20 = -25 ± 3º (C=1 en DMF) D 20 = -38 ± 3º (C=1 en EtOH)
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
-
Aplicaciones

Fmoc-L-octahydroindole-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and improving yield and purity.
  • Drug Development: Its structural properties make it valuable in the design of novel pharmaceuticals, particularly in the development of compounds targeting neurological conditions.
  • Bioconjugation: The chemical is employed in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Material Science: It is used in the creation of advanced materials, particularly in the development of polymers with specific functionalities for applications in coatings and adhesives.
  • Research in Organic Chemistry: The compound is a key reagent in various organic synthesis pathways, providing researchers with a versatile tool for exploring new chemical reactions.

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