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Fmoc-4-azidophenylalanine

Fmoc-4-azidophenylalanine

Item no.	AS-64347-1000
Manufacturer	AnaSpec
Amount	1 g
Category	Peptides & Proteins Amino Acids
Type	Amino Acids
Specific against	other
Citations	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-alpha-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.
ECLASS 10.1	32160406
ECLASS 11.0	32160406
UNSPSC	12352209
Alias	Fmoc-Phe(N3)-OH; Fmoc-p-azidophenylalanine; Fmoc-phenylalanine-azide
Available
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
MF	C24 H20 N4 O4
MW	428, 44
Product Group	RE1C1C
Shipping	RT
Storage	4 C

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

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Amount: 1 g

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