Fmoc-L-Sec(Mob)-OH

Hazmat

Chemical name: N-alpha-(9-Fluorenylmethyloxycarbonyl)-Se-(4-methoxybenzyl)-L-selenocysteine // Synonyms: Fmoc-L-Sec(pMeOBzl)-OH, Fmoc-L-Sec(Pmb)-OH, Fmoc-Sec(Mob), Fmoc-L-4-methoxybenzyl selenocysteine,(2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-3-[4-methoxybenzyl)selanyl]propionic acid, Fmoc-Sec( MPM), (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)a

  • Product code:FAA8705
  • CAS No.:150308-80-8
  • Formula:C26H25NO5Se
  • Storage temperature:2-8°C
  • Molecular weight:510.46 g/mol
  • Purity :min. 99%
  • Enantiomeric Purity:min. 99.9%

from €90.00

Grouped product items
Qty Packing unit Price SKU Availability
100 mg
€90.00
FAA8705.0100
<10 business days
250 mg
€150.00
FAA8705.0250
<10 business days
500 mg
€270.00
FAA8705.0500
<10 business days
1 g
€420.00
FAA8705.1000
<10 business days
5 g
€1,500.00
FAA8705.5000
<10 business days
Safety Data Sheets
description

Building block for the introduction of selenocysteine by SPPS. Peptides containing selenocysteine can be cleaved from the resin with simultaneous side-chain deprotection by treatment with 5% (v/v) water, 95% (v/v) trifluoroacetic acid (TFA), 0.4 M 2,2’-dithiobis(5-nitropyridine) (DTNP) for 7 min at 60 °C or 2 h at RT. See also FAA8710 Fmoc-D-Sec(Mob)-OH.


references

A chemoselective strategy for late-stage functionalization of complex small molecules with polypeptides and proteins; D. T. Cohen, C. Zhang, C. M. Fadzen, A. J. Mijalis, L. Hie, K. D. Johnson, Z. Shriver, O. Plante, S. J. Miller, S. L. Buchwald, B. L. Pentelute;

Nat. Chem. 2019; 11: 78-85. https://doi.org/10.1038/s41557-018-0154-0.


Chemical synthesis of ferredoxin with 4 selenocysteine residues using a segment condensation method; T. Takei, T. Ando, T. Takao, Y. Ohnishi, G. Kurisu, M. Iwaoka, H. Hojo; Chem. Commun. 2020; 56: 14239-14242; https://doi.org/10.1039/D0CC06252A.


Reassessment of an Innovative Insulin Analogue Excludes Protracted Action yet Highlights the Distinction between External and Internal Diselenide Bridges; B. Dhayalan, Y.-S. Chen, N. B. Phillips, M. Swain, N. K. Rege, A. Mirsalehi, M. Jarosinski, F. Ismail-Beigi, N. Metanis, M. A. Weiss; Chem. Eur. J. 2020; 26(21): 4695-4700. https://doi.org/10.1002/chem.202000309.


Copper-Mediated Selenazolidine Deprotection Enables One-Pot Chemical Synthesis of Challenging Proteins; Z. Zhao, N. Metanis; Angew. Chem. Int. Ed. 2019; 58(41): 14610-14614. https://doi.org/10.1002/anie.201909484. 

* Disclaimer
We refer to our general terms and conditions.
All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.

Do you need further information about this product?

get in contact

Quick contact

Please send me more information about

We found other products you might like!