Descubra el nuevo Chem-Impex: donde la innovación comienza con un vínculo.

Catalog Number:
02684
CAS Number:
117014-32-1
Éster β-9-fluorenilmetílico del ácido Boc-L-aspártico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-Asp(OFm)-OH
Documents
$110.57 /1G
Tamaño
Request Bulk Quote
Información del producto

Boc-L-aspartic acid b-9-fluorenylmethyl ester is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for complex organic synthesis. The fluorenylmethyl ester moiety provides additional protection and facilitates the purification of peptides, allowing for more efficient synthesis processes.

Researchers and industry professionals can leverage Boc-L-aspartic acid b-9-fluorenylmethyl ester in the development of bioactive peptides, drug candidates, and various therapeutic applications. Its unique structure not only aids in the formation of stable peptide bonds but also enhances the overall yield of synthesis reactions. This compound is particularly valuable in the fields of medicinal chemistry and biochemistry, where precision and efficiency are paramount. With its robust properties and practical applications, Boc-L-aspartic acid b-9-fluorenylmethyl ester stands out as a key reagent for advancing research and development in peptide chemistry.

Número CAS
117014-32-1
Fórmula molecular
C23H25NO6
Peso molecular
411.5
Número MDL
MFCD00076916
Rotación óptica
[a] D 20 = 26 ± 2 º (C=1 en MeOH)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
117014-32-1
Fórmula molecular
C23H25NO6
Peso molecular
411.5
Número MDL
MFCD00076916
Rotación óptica
[a] D 20 = 26 ± 2 º (C=1 en MeOH)
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

Boc-L-aspartic acid b-9-fluorenylmethyl 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, allowing for the creation of complex proteins with specific functionalities.
  • Drug Development: Its derivatives are explored in pharmaceutical research for developing new drugs, especially those targeting neurological disorders, due to its structural similarity to neurotransmitters.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, enhancing the efficacy of drug delivery systems.
  • Research in Biochemistry: It plays a significant role in studying enzyme mechanisms and protein interactions, providing insights into metabolic pathways and cellular functions.
  • Material Science: The compound is also investigated for its potential applications in creating novel materials, such as hydrogels, which can be used in tissue engineering and regenerative medicine.

Citas