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Catalog Number:
02424
CAS Number:
122996-47-8
Fmoc- O - terc -butil-L- trans -4-hidroxiprolina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Hip(tBu)-OH
Documents
$25.00 /1G
Tamaño
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Información del producto

Fmoc-O-tert-butyl-L-trans-4-hydroxyproline is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis process, making it an invaluable tool for chemists working in the field of medicinal chemistry. Its unique structure, characterized by the tert-butyl group, enhances solubility and stability, facilitating its use in various organic reactions.

Researchers and industry professionals can leverage Fmoc-O-tert-butyl-L-trans-4-hydroxyproline in the design of bioactive peptides, particularly in the development of therapeutics targeting neurological disorders and other diseases. Its ability to provide a stable backbone while allowing for functional group modifications makes it an ideal candidate for creating complex peptide libraries. Additionally, its favorable properties compared to other amino acid derivatives can lead to improved yields and purities in peptide synthesis, making it a preferred choice for both academic and industrial applications.

Número CAS
122996-47-8
Fórmula molecular
C 24 H 27 N º 5
Peso molecular
409.48
Número MDL
MFCD00151930
Rotación óptica
[a] D 20 = -25 ± 2 º (C=1 en MeOH)
Condiciones
Conservar a ≤ 4 °C
Información general
Número CAS
122996-47-8
Fórmula molecular
C 24 H 27 N º 5
Peso molecular
409.48
Número MDL
MFCD00151930
Rotación óptica
[a] D 20 = -25 ± 2 º (C=1 en MeOH)
Condiciones
Conservar a ≤ 4 °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-O-tert-butyl-L-trans-4-hydroxyproline is widely utilized in research focused on:

  • Peptide Synthesis: This compound is commonly used as a building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, due to its stability and ease of removal during deprotection steps.
  • Drug Development: It plays a crucial role in the development of pharmaceuticals, especially in creating compounds that target specific biological pathways, enhancing the efficacy of drug candidates.
  • Bioconjugation: The chemical is valuable in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential for creating targeted therapies and diagnostics.
  • Protein Engineering: In protein engineering, it helps in modifying proteins to improve their stability and functionality, making it easier to design proteins with desired characteristics for industrial applications.
  • Research in Structural Biology: It is utilized in the study of protein structures, aiding in the understanding of protein folding and interactions, which is vital for advancing knowledge in biochemistry and molecular biology.

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