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Catalog Number:
31670
CAS Number:
1795781-13-3
Acide ( S )-Fmoc-2-amino-5-(2-méthyl-1,3-dioxolan-2-yl)-pentanoïque
Purity:
≥ 99 % (HPLC)
Documents
$86.23 /25 mg
Taille
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Product Information

(S)-Fmoc-2-amino-5-(2-methyl-1,3-dioxolan-2-yl)-pentanoic acid is a versatile building block 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 acids during solid-phase peptide synthesis. Its unique structure, incorporating a dioxolane moiety, enhances its stability and solubility, making it an ideal choice for researchers focused on synthesizing complex peptides and pharmaceuticals.

In the realm of medicinal chemistry, (S)-Fmoc-2-amino-5-(2-methyl-1,3-dioxolan-2-yl)-pentanoic acid serves as a crucial intermediate in the development of bioactive compounds, particularly those targeting specific biological pathways. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups positions it as a preferred option for professionals seeking efficiency and reliability in their synthetic processes. This compound not only streamlines the synthesis of peptides but also opens avenues for innovative drug design, making it a valuable asset in both academic and industrial laboratories.

CAS Number
1795781-13-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C 24 H 276
Molecular Weight
425.48
MDL Number
MFCD30749169
PubChem ID
138108767
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = -13 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
CAS Number
1795781-13-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C 24 H 276
Molecular Weight
425.48
MDL Number
MFCD30749169
PubChem ID
138108767
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = -13 ± 2º (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

(S)-Fmoc-2-amino-5-(2-methyl-1,3-dioxolan-2-yl)-pentanoic 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, allowing for the creation of complex and diverse peptide structures.
  • Drug Development: Its unique structure makes it valuable in pharmaceutical research, particularly for developing peptide-based drugs that can target specific biological pathways.
  • Bioconjugation: The compound can be used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: It is applied in studies related to neuropeptides, contributing to the understanding of neurological functions and potential treatments for neurological disorders.
  • Analytical Chemistry: This chemical is utilized in analytical methods to study protein interactions and stability, helping researchers gain insights into protein behavior under various conditions.

Citations