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Details
Allylglycine-containing peptides may be cleaved selectively at the amide bond between allylglycine and the subsequent amino acid with iodine. The lateral double bond allows selective modifications of a peptide e.g. via metathesis. Replacing cysteine residues by allylglycine allows to obtain carba-analogs of disulfide-bridged peptides.
Educt for obtaining Fmoc-prenylglycine.
Educt for obtaining Fmoc-prenylglycine.
Catalog Number
B-4190
Synonyms
(S)-2-Fmoc-amino-4-pentenoic acid, Fmoc-L-allylglycine
Molecular Formula
C₂₀H₁₉NO₄
Relative Molecular Mass
337.38
CAS Registry Number
[146549-21-5]
Storage Conditions
-20 ± 5 °C
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