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Catalog Number:
29323
CAS Number:
102971-73-3
Ácido R -Fmoc-2-amino-3-(3- tert -butoxicarbonil-propilsulfanil)propiónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Cys( terc- butoxicarbonilpropil)-OH
Documents
$72.31 /100 mg
Tamaño
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Información del producto

(R)-Fmoc-2-amino-3-(3-tert-butoxycarbonyl-propylsulfanyl)propionic acid is a versatile amino acid derivative widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, which includes a tert-butoxycarbonyl group and a sulfanyl side chain, enhances its stability and solubility, making it an ideal choice for researchers focused on developing complex peptide sequences.

In practical applications, (R)-Fmoc-2-amino-3-(3-tert-butoxycarbonyl-propylsulfanyl)propionic acid serves as a key building block in the production of bioactive peptides, pharmaceuticals, and therapeutic agents. Its ability to facilitate the formation of disulfide bonds and its compatibility with various coupling reagents make it particularly valuable in the synthesis of cyclic peptides and other advanced biomolecules. Researchers and industry professionals can leverage this compound to streamline their synthesis processes and enhance the efficacy of their peptide-based products.

Número CAS
102971-73-3
Fórmula molecular
C26H31NO6S
Peso molecular
485.6
Número MDL
MFCD11226818
Punto de fusión
88 - 95 °C
Rotación óptica
[a] D 20 = -30 ± 2 º (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
102971-73-3
Fórmula molecular
C26H31NO6S
Peso molecular
485.6
Número MDL
MFCD11226818
Punto de fusión
88 - 95 °C
Rotación óptica
[a] D 20 = -30 ± 2 º (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

(R)-Fmoc-2-amino-3-(3-tert-butoxycarbonyl-propylsulfanyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without affecting other functional groups.
  • Drug Development: Its unique structure aids in the design of novel peptides and peptidomimetics, which can lead to the development of new therapeutic agents in pharmaceuticals.
  • Bioconjugation: The compound can be used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Research in Protein Engineering: It plays a significant role in protein engineering, where its properties help in modifying proteins for enhanced stability and activity, benefiting fields like biotechnology.
  • Analytical Chemistry: This chemical is also employed in analytical techniques for the characterization of complex mixtures, providing insights into molecular interactions and structures.

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