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Catalog Number:
03613
CAS Number:
146982-24-3
Ester β-allylique de l'acide Fmoc-L-aspartique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Asp(OAll)-OH
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Product Information

Fmoc-L-aspartic acid b-allyl ester is a versatile building block widely utilized in peptide synthesis and organic chemistry. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential tool for researchers in the field of medicinal chemistry and drug development. Its unique b-allyl ester functionality enhances its reactivity, facilitating the formation of complex peptide structures with improved yields and purity.

In addition to its role in peptide synthesis, Fmoc-L-aspartic acid b-allyl ester is also valuable in the development of bioactive compounds and pharmaceuticals. Its ability to participate in various coupling reactions makes it suitable for creating diverse molecular architectures, which can lead to the discovery of new therapeutic agents. Researchers appreciate its stability and compatibility with a range of reaction conditions, making it a reliable choice for both academic and industrial applications.

Synonyms
Fmoc-L-Asp(OAll)-OH
CAS Number
146982-24-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 216
Molecular Weight
395.4
MDL Number
MFCD00190874
PubChem ID
5228830
Melting Point
109 - 120 °C
Appearance
Poudre blanche ou poudre cristalline blanche
Optical Rotation
[a] 20 D = -27 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-Asp(OAll)-OH
CAS Number
146982-24-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 216
Molecular Weight
395.4
MDL Number
MFCD00190874
PubChem ID
5228830
Melting Point
109 - 120 °C
Appearance
Poudre blanche ou poudre cristalline blanche
Optical Rotation
[a] 20 D = -27 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 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-aspartic acid b-allyl ester 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 is used in the design of pharmaceutical compounds, particularly in the development of drugs targeting neurological disorders, due to its ability to modify amino acids effectively.
  • Bioconjugation: The chemical is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted therapies.
  • Research in Protein Engineering: It plays a significant role in protein engineering, helping scientists to modify proteins for enhanced stability or activity, which is vital for therapeutic applications.
  • Analytical Chemistry: This compound is used in analytical methods to study protein interactions and behaviors, providing insights that are essential for various biochemical research projects.

Citations