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Catalog Number:
33487
CAS Number:
273222-05-2
Fmoc-L-Pro(4-NH-Aloc)-OH (2 S ,4 R
Purity:
98 - 101 % (dosage par titrage)
Synonym(s):
Acide (2S,4 R -4-allyloxycarbonylamino-1-(9-fluorénylméthyloxycarbonyl)-pyrrolidine-2-carboxylique
Documents
$100.05 /25 mg
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Product Information

Fmoc-L-Pro(4-NH-Aloc)-OH (2S,4R) is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of complex peptides. Its unique structure, characterized by the presence of an allyloxycarbonyl group, enhances its reactivity and stability, making it an ideal choice for researchers looking to create high-purity peptides with specific functionalities.

In the pharmaceutical industry, Fmoc-L-Pro(4-NH-Aloc)-OH is particularly valuable for the synthesis of bioactive peptides, which can serve as potential therapeutics or research tools. Its ability to facilitate the introduction of various functional groups allows for the customization of peptides, thereby expanding their applications in drug discovery and development. Researchers appreciate its compatibility with automated synthesizers, which streamlines the peptide synthesis process and improves efficiency. Overall, this compound stands out for its practical applications in both academic and industrial settings, offering significant advantages over traditional amino acid derivatives.

Synonyms
Acide (2S,4 R -4-allyloxycarbonylamino-1-(9-fluorénylméthyloxycarbonyl)-pyrrolidine-2-carboxylique
CAS Number
273222-05-2
Purity
98 - 101 % (dosage par titrage)
Molecular Formula
C24H24N2O6
Molecular Weight
436.5
MDL Number
MFCD08704529
PubChem ID
76045159
Melting Point
160 - 168 ?C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] 20 D = -9 ± 1 ° (C=1 dans MeOH)
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Acide (2S,4 R -4-allyloxycarbonylamino-1-(9-fluorénylméthyloxycarbonyl)-pyrrolidine-2-carboxylique
CAS Number
273222-05-2
Purity
98 - 101 % (dosage par titrage)
Molecular Formula
C24H24N2O6
Molecular Weight
436.5
MDL Number
MFCD08704529
PubChem ID
76045159
Melting Point
160 - 168 ?C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] 20 D = -9 ± 1 ° (C=1 dans MeOH)
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-L-Pro(4-NH-Aloc)-OH (2S,4R) is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities.
  • Drug Development: It plays a crucial role in developing pharmaceuticals, particularly in designing peptide-based drugs that can target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted therapies.
  • Research in Protein Engineering: It aids in the modification of proteins, enhancing their stability and activity, which is vital for various applications in biotechnology.
  • Diagnostic Applications: The compound can be utilized in the development of diagnostic tools, particularly in assays that require specific peptide interactions for disease detection.

Citations