Molecular structure of Fmoc-Gly-OH, CAS Number: 29022-11-5
Fmoc-Gly-OH (CAS 29022-11-5)
Alternate Names:
Fmoc-glycine
Application:
Fmoc-Gly-OH is an Fmoc protected glycine derivative
CAS Number:
29022-11-5
Molecular Weight:
297.31
Molecular Formula:
C17H15NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Fmoc-Gly-OH is an Fmoc protected glycine derivative useful for proteomics studies and solid phase peptide synthesis techniques. Glycine is the simplest, and least sterically hindered of the amino acids, which confers a high level of flexibility when incorporated into polypeptides. This compound could be useful for solid phase peptide synthesis and for coupling of saccharide beta-glycosylamines used for the for the fractionation of oligosaccharides and formation of neoglycoconjugates.
Fmoc-Gly-OH (CAS 29022-11-5) References
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- 'O-Acyl isopeptide method' for peptide synthesis: Solvent effects in the synthesis of Abeta1-42 isopeptide using 'O-acyl isodipeptide unit'. | Taniguchi, A., et al. 2007. J Pept Sci. 13: 868-74. PMID: 17803257
- Dicyclopropylmethyl peptide backbone protectant. | Carpino, LA., et al. 2009. Org Lett. 11: 3718-21. PMID: 19719204
- Rhodamine-marked bombesin: a novel means for prostate cancer fluorescence imaging. | Sturzu, A., et al. 2014. Invest New Drugs. 32: 37-46. PMID: 23728918
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- Serine-selective aerobic cleavage of peptides and a protein using a water-soluble copper-organoradical conjugate. | Seki, Y., et al. 2014. Angew Chem Int Ed Engl. 53: 6501-5. PMID: 24826926
- Efficient Method for the Concentration Determination of Fmoc Groups Incorporated in the Core-Shell Materials by Fmoc-Glycine. | Szczepańska, E., et al. 2020. Molecules. 25: PMID: 32882948
- Amino-acids condensations in the preparation of N alpha-9-fluorenylmethyloxycarbonylamino-acids with 9-fluorenylmethylchloroformate. | Tessier, M., et al. 1983. Int J Pept Protein Res. 22: 125-8. PMID: 6885246
- Model studies on protease-catalysed peptide synthesis using 9-fluorenylmethoxycarbonyl protected amino acid derivatives | Peter Kuhl, Simone Säuberlich & Hans-Dieter Jakubke. 1992. Monatshefte für Chemie / Chemical Monthly. 123: 1015–1022.
- Preservation of the protective group under alkaline conditions by using CaCl2. Applications in peptide synthesis | Robert Pascal ∗ 1, Régine Sola. 1998. Tetrahedron Letters. 39: 5031-5034.
- Monitoring solid phase reactions with ion-selective electrode | Marcel Pátek *, Sylvia Bildstein, Zuzana Flegelová. 1998. Tetrahedron Letters. 39: 753-756.
- Oxime Carbonates: Novel Reagents for the Introduction of Fmoc and Alloc Protecting Groups, Free of Side Reactions | Sherine N. Khattab, Ramon Subirós-Funosas, Ayman El-Faham, Fernando Albericio. 2010. European Journal of Organic Chemistry. 2010: 3275-3280.
- A novel conducting copolymer: Investigation of its matrix properties for cholesterol biosensor applications | Saniye Soylemez a, Fulya Ekiz Kanik b, Ayda Goyçek Nurioglu a, Hava Akpinar c, Levent Toppare a b c d. 2013. Sensors and Actuators B: Chemical. 182: 322-329.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fmoc-Gly-OH, 5 g | sc-255183 | 5 g | $22.00 |