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Catalog Number:
33486
CAS Number:
274676-10-7
Fmoc-L-Pro(4-NH-Aloc)-OH ( 2S ,4S )
Purity:
98 - 101% (Ensayo por titulación)
Synonym(s):
Ácido (2 S ,4 S -4-aliloxicarbonilamino-1-(9-fluorenilmetiloxicarbonil)-pirrolidin-2-carboxílico
Documents
$89.50 /100 mg
Tamaño
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Product Information

Fmoc-L-Pro(4-NH-Aloc)-OH is a specialized amino acid derivative that serves as a crucial building block in peptide synthesis and drug development. This compound, known for its high purity and stability, features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which facilitates the selective deprotection of amino acids during the synthesis process. Its unique structure, characterized by the presence of an allyloxycarbonyl (Aloc) group, enhances its utility in the formation of complex peptides and proteins, making it an invaluable tool for researchers in medicinal chemistry and biochemistry.

The practical applications of Fmoc-L-Pro(4-NH-Aloc)-OH extend to the development of peptide-based therapeutics and the study of protein interactions. Its ability to provide a stable and versatile platform for the synthesis of modified peptides allows researchers to explore new therapeutic avenues, particularly in the fields of oncology and immunology. With its favorable properties, this compound stands out among similar products, offering enhanced efficiency and reliability in peptide synthesis protocols.

Synonyms
Ácido (2 S ,4 S -4-aliloxicarbonilamino-1-(9-fluorenilmetiloxicarbonil)-pirrolidin-2-carboxílico
CAS Number
274676-10-7
Purity
98 - 101% (Ensayo por titulación)
Molecular Formula
C24H24N2O6
Molecular Weight
436.5
MDL Number
MFCD22989434
PubChem ID
76045159
Melting Point
128 - 136 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] 20 D = -28 ± 2 º (C=1 en DMF)
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Ácido (2 S ,4 S -4-aliloxicarbonilamino-1-(9-fluorenilmetiloxicarbonil)-pirrolidin-2-carboxílico
CAS Number
274676-10-7
Purity
98 - 101% (Ensayo por titulación)
Molecular Formula
C24H24N2O6
Molecular Weight
436.5
MDL Number
MFCD22989434
PubChem ID
76045159
Melting Point
128 - 136 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] 20 D = -28 ± 2 º (C=1 en DMF)
Conditions
Conservar entre 2 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-L-Pro(4-NH-Aloc)-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups. This is crucial for creating complex peptides used in pharmaceuticals.
  • Drug Development: Its unique structure aids in the design of peptide-based drugs, particularly in targeting specific biological pathways. Researchers can create more effective therapeutics by leveraging its properties.
  • Bioconjugation: The compound is useful in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the effectiveness of diagnostics and drug delivery systems.
  • Research in Protein Engineering: It is employed in the modification of proteins to study their structure and function, providing insights into protein interactions and stability, which is vital for developing new biotechnological applications.
  • Academic Research: Many academic laboratories utilize this compound for experimental studies in organic chemistry and biochemistry, facilitating advancements in understanding molecular interactions and reactions.

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