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β-Amino Acids
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Analogs of Alanine, Glycine, Valine, and Leucine
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Analogs of Phenylalanine and Tyrosine
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Aromatic Amino Acids
Azide and Alkyne containing Amino Acids
Building Blocks for Stapled Peptides
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  Product  Fmoc - 4 - azidophenylalanineFmoc - Phe(N3) - OH;
  Fmoc - p - azidophenylalanine; Fmoc - phenylalanine - azide
  CAS  Fmoc - p - azidophenylalanine; Fmoc - phenylalanine - azide
  Size  1 g
  Catalog #  64347-1000
  US$  484
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Description

An unusual amino acid used in Solid Phase Peptide Synthesis (SPPS) for the synthesis of photoreactive affinity labels.1,2,3 The side-chain azido (N3) group is stable in trifluoroacetic acid (TFA) or piperidine (Pip), two reagents commonly used in SPPS. The azido group can be readily converted to an amine on the solid phase or in solution via the Staudinger reduction.4

Detailed Information Flyer
Storage 4°C
References 1. Schwyzer, R.; Caviezel, M. p-Azido-L-phenylalanine: A photo-affinity ‘probe’ related to tyrosine.Helvetica. Chim. Acta.1971 (54) 1395-1400. 
2. Fahrenholz, F.; Thierauch, K. H. Synthesis of p-Amino-L-Phenylalanine derivatives with protected p-amino group for the preparation of p-azido-L-phenylalanine peptides.Inter. J. Pept. & Prot. Res.1980 (15) 323-330. 
3. Fahrenholz, F.; Toth, G.; Crause, P.; Eggena, P.; Schwartz, I. L. [1,6-α-Aminosuberic Acid, 3-(p-Azidophenylalanine, 8-Arginine] Vasopressin: A New Photoaffinity Label for Hydroosmotic Hormone Receptors. J. Biol. Chem.1983 (258) 14861-14867. 
4. Staudinger, H.; Meyer, J. UberneueorganischePhosphorverbindungen III. Phosphinmethylenederivative und Phosphinimine. Helvetica Chim. Acta. 1919 (2) 635-646.
Molecular Weight 428.44
Molecular Formula C24 H20 N4 O4


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