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Catalog Number:
04074
CAS Number:
218457-76-2
Acide Fmoc-L-α-aminosubérique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Asu-OH, Acide Fmoc-L-2-aminooctanedioïque
Documents
$181.67 /100 mg
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Product Information

Fmoc-L-a-aminosuberic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which facilitates the selective modification of amino acids during the synthesis process. Its unique structure, characterized by an octanedioic acid backbone, enhances its solubility and reactivity, making it an ideal choice for researchers focusing on the development of complex peptides and biologically active compounds.

In practical applications, Fmoc-L-a-aminosuberic acid is particularly valuable in the pharmaceutical industry for the synthesis of peptide-based therapeutics. Its ability to serve as a chiral building block allows for the creation of enantiomerically pure compounds, which are crucial in drug formulation. Additionally, its stability under various reaction conditions makes it a reliable choice for both academic and industrial laboratories. Researchers can leverage this compound to streamline their synthesis processes, ultimately leading to more efficient development of novel therapeutic agents.

Synonyms
Fmoc-L-Asu-OH, Acide Fmoc-L-2-aminooctanedioïque
CAS Number
218457-76-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C 23 H 256
Molecular Weight
411.46
MDL Number
MFCD01317728
PubChem ID
46737326
Melting Point
154 - 159 ?C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 20 D = -1,5 ± 0,5 ° (C=1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-L-Asu-OH, Acide Fmoc-L-2-aminooctanedioïque
CAS Number
218457-76-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C 23 H 256
Molecular Weight
411.46
MDL Number
MFCD01317728
PubChem ID
46737326
Melting Point
154 - 159 ?C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 20 D = -1,5 ± 0,5 ° (C=1 dans MeOH)
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-a-aminosuberic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, enhancing the efficiency and yield of the process.
  • Drug Development: It plays a significant role in the pharmaceutical industry for developing novel drug candidates, especially those targeting specific biological pathways.
  • Bioconjugation: Its functional groups allow for effective bioconjugation, making it valuable in creating targeted therapies and diagnostic agents in biomedicine.
  • Research in Neuroscience: The compound is used in studies related to neuropeptides, contributing to the understanding of neurological functions and disorders.
  • Material Science: It is also explored in the development of new materials, particularly in creating polymers with specific properties for various applications.

Citations