Comparison

(2S)-N-Fmoc-5-azido-pentanoic acid

Item no. AS-65518-1
Manufacturer AnaSpec
CASRN 1097192-04-5
Amount 1 g
Category
Type Amino Acids
Specific against other
Citations 1. Vallee, MRJ. et al. (2011). Staudinger-Phosphonite Reactions for the Chemoselective Transformation of Azido-Containing Peptides and Proteins. Org Lett 13, 5440.2. Staudinger, H. & Meyer, J. (1919). Uberneueorganische Phosphorverbindungen III. Phosphinmethylenederivative und Phosphinimine. Helvetica Chim Acta 2, 635.3. Oh, K-I. et al. (2008). ß-Azidoalanine as an IR Probe: Application to Amyloid Aß (16-22) Aggregation. J Phys Chem B 112, 10352.
ECLASS 10.1 32160406
ECLASS 11.0 32160406
UNSPSC 12352209
Alias 1097192-04-5
Similar products 1097192-04-5
Available
Description
This unusual amino acid is used in Solid Phase Peptide Synthesis (SPPS) for the synthesis of modifiable side-chain peptides and proteins.1 The side-chain azido (N3) group is stable in trifluoroacetic acid (TFA) and 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 Staudinger reduction.2 In addition, incorporation of azidohomoalanine into proteins has shown promise as an effective IR probe of local electrostatic environments in proteins.3
MF
C20H20N4O4
MW
380, 4
Product Group
RE1C1C
Shipping
RT
Storage
-20C

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.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 1 g
Available: In stock
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