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Catalog Number:
26461
CAS Number:
223581-83-7
Fmoc-Pro(4-ceto)-OH
Purity:
≥ 99 % (HPLC, TLC)
Synonym(s):
Fmoc-Pro(4-ceto)
Documents
$93.14 /100 mg
Tamaño
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Product Information

Fmoc-Pro(4-keto)-OH is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique 4-keto structure enhances the stability and reactivity of the compound, making it an ideal choice for researchers looking to streamline their synthesis processes. Fmoc-Pro(4-keto)-OH is particularly valuable in the development of bioactive peptides and pharmaceuticals, where precise control over amino acid sequences is critical.

In addition to its applications in peptide synthesis, this compound can also be employed in the study of protein interactions and the development of novel therapeutic agents. Its ability to facilitate the formation of complex structures allows researchers to explore new avenues in drug design and molecular biology. With its favorable properties and broad applicability, Fmoc-Pro(4-keto)-OH stands out as a crucial tool for professionals in the fields of chemistry and biochemistry.

Synonyms
Fmoc-Pro(4-ceto)
CAS Number
223581-83-7
Purity
≥ 99 % (HPLC, TLC)
Molecular Formula
C 20 H 17 N.º 5
Molecular Weight
351.4
MDL Number
MFCD01632258
PubChem ID
18545225
Melting Point
77 - 88 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = + 10,9 ± 1º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-Pro(4-ceto)
CAS Number
223581-83-7
Purity
≥ 99 % (HPLC, TLC)
Molecular Formula
C 20 H 17 N.º 5
Molecular Weight
351.4
MDL Number
MFCD01632258
PubChem ID
18545225
Melting Point
77 - 88 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = + 10,9 ± 1º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-Pro(4-keto)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the solid-phase synthesis of peptides, enabling researchers to create complex peptide sequences efficiently.
  • Drug Development: Its unique structure allows for modifications that can enhance the bioactivity of pharmaceutical compounds, making it valuable in the design of new drugs.
  • Bioconjugation: The chemical's reactive groups facilitate the attachment of biomolecules, aiding in the development of targeted therapies and diagnostic tools in the biomedical field.
  • Research in Protein Engineering: It is used to modify amino acids in proteins, helping scientists study protein function and interactions, which is crucial for understanding diseases.
  • Material Science: The compound can be incorporated into polymer systems, improving their properties for applications in coatings and drug delivery systems.

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