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

Catalog Number:
02454
CAS Number:
71989-33-8
Fmoc -O - tert -butil-L-serina
Purity:
≥ 99,5 % (HPLC quiral, HPLC)
Synonym(s):
Fmoc-L-Ser(tBu)-OH
Documents
$25.00 /5G
Tamaño
Request Bulk Quote
Información del producto

Fmoc-O-tert-butyl-L-serine is a versatile amino acid derivative widely utilized in peptide synthesis and bioconjugation applications. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential building block for researchers in the field of medicinal chemistry and drug development. Its tert-butyl group enhances solubility and stability, facilitating smoother reactions and improving yields in complex synthetic pathways.

Researchers and industry professionals appreciate Fmoc-O-tert-butyl-L-serine for its role in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. This compound is particularly advantageous in solid-phase peptide synthesis (SPPS), where its protective groups can be easily removed under mild conditions, allowing for the efficient assembly of peptides. Its unique properties make it a preferred choice for those looking to streamline their synthesis processes while achieving high purity and functionality in their final products.

Número CAS
71989-33-8
Fórmula molecular
C22H25Nº 5
Peso molecular
383.4
Número MDL
MFCD00037127
Punto de fusión
125 - 140 °C
Rotación óptica
[a] D 20 = 25 ± 3 º (C=1 en EtOAc)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
71989-33-8
Fórmula molecular
C22H25Nº 5
Peso molecular
383.4
Número MDL
MFCD00037127
Punto de fusión
125 - 140 °C
Rotación óptica
[a] D 20 = 25 ± 3 º (C=1 en EtOAc)
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

Fmoc-O-tert-butyl-L-serine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group for the amino acid serine during peptide synthesis, allowing for the selective modification of other amino acids without affecting serine.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in the development of drugs targeting specific biological pathways.
  • Bioconjugation: Researchers use it to facilitate the attachment of biomolecules to surfaces or other molecules, enhancing the efficacy of diagnostics and therapeutics.
  • Protein Engineering: The compound is used in the modification of proteins to improve their stability and functionality, which is essential in various biotechnological applications.
  • Research in Neuroscience: It is applied in studies involving neurotransmitter systems, where modified peptides can help in understanding receptor interactions and signaling pathways.

Citas