Fmoc 4-azido-L-phenylalanine
Fmoc protected Azidophenylalanine for biochemistry, protein synthesis, expression etc.
From the laboratory of Matthew I. Gibson, PhD, University of Warwick.
Fmoc protected Azidophenylalanine for biochemistry, protein synthesis, expression etc.
From the laboratory of Matthew I. Gibson, PhD, University of Warwick.
| Catalog Number | Product | DataSheet | Size | AVAILABILITY | Price | Qty |
|---|
Specifications
| Product Type: | Small Molecule |
| Name: | Fmoc-Phe(4-N3)-OH |
| Chemical Formula: | C24H20N4O4 |
| CAS number: | 163217-43-4 |
| Molecular Weight: | 428.45 g/mol-1 |
| Format: | Orange-brown powder |
| Purity: | >98% HPLC |
| Solubility: | DMSO, DMF; Organic Solvents. Insoluble in H2O, MeOH, ACN |
| Spectral Information: | 1H/13C NMR, LCMS, and HPLC (see Documentation below) |
| Comments: | Protect from light and shock |
| Storage: | -20C |
| Shipped: | Cold Packs |
Documentation
Provider
From the laboratory of Matthew I. Gibson, PhD, University of Warwick.
References
- Schwyzer R, Caviezel M. p-Azido-L-phenylalanine: a photo-affinity 'probe' related to tyrosine. Helv Chim Acta. 1971;54(5):1395-400. PubMed PMID: 5121750.
- Fahrenholz F, Thierauch KH. Synthesis of p-amino-L-phenylalanine derivatives with protected p-amino group for preparation of p-azido-L-phenylalanine peptides. Int J Pept Protein Res. 1980 Apr;15(4):323-30. PubMed PMID: 7419359.
- Chin JW, Santoro SW, Martin AB, King DS, Wang L, Schultz PG. Addition of p-azido-L-phenylalanine to the genetic code of Escherichia coli. J Am Chem Soc. 2002 Aug 7;124(31):9026-7. PubMed PMID: 12148987.
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