Alloc-Aeg(Fmoc)-OH

Nom chimique: N-alpha-Allyloxycarbonyl-N-(2-(9-Fluorenylmethyloxycarbonyl)aminoethyl)-glycine // Synonymes: Fmoc-Aeg(Alloc), Alloc-N-(2-Fmoc-aminoethyl)-glycine, Aloc-Aeg(Fmoc)-OH

  • n° Art.:AAA2200
  • n° CAS:570383-98-1
  • Formule:C23H24N2O6
  • Storage temperature:2-8°C
  • Masse moléculaire:424,45 g/mol
  • Pureté:min. 99%

from 108,00 €

Grouped product items
Nombre Unité de vente Prix SKU Disponibilité
500 mg
108,00 €
AAA2200.0500
<10 jour ouvrables
1 g
168,00 €
AAA2200.1000
<10 jour ouvrables
5 g
600,00 €
AAA2200.5000
<10 jour ouvrables
Fiches de données de sécurité
description

Trifunctional building block for peptoid synthesis and a variety of other reactions (peptidomimetics, linker with branching functionality, heterocycles).

This compound is a potential building block for the construction of (customized) peptide nucleic acids (PNAs) and for peptoid synthesis.



references

Optimization of the Alkyl Linker of TO Base Surrogate in Triplex-Forming PNA for Enhanced Binding to Double-Stranded RNA; T. Sato, Y. Sato, S. Nishizawa; Chem. Eur. J. 2017; 23(17): 4079-4088. https://doi.org/10.1002/chem.201604676.


Triplex-Forming Peptide Nucleic Acid Probe Having Thiazole Orange as a Base Surrogate for Fluorescence Sensing of Double-stranded RNA; T. Sato, Y. Sato, S. Nishizawa; J. Am. Chem. Soc. 2016; 138(30): 9397-9400. https://doi.org/10.1021/jacs.6b05554.


DNA-Templated Synthesis of Trimethine Cyanine Dyes: A Versatile Fluorogenic Reaction for Sensing G-Quadruplex Formation; K. Meguellati, G. Koripelly, S. Ladame; Angew. Chem. Int. Ed. 2010; 49(15): 2738-2742. https://doi.org/10.1002/anie.201000291.

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