Fmoc-Pra-OH

CAS: 198561-07-8

Ref. 01-4053914

Produktinformation

• Name: Fmoc-Pra-OH
• Synonyme: Fmoc-Propargyl-Gly-OH, (2R)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}pent-4-ynoic acid, (2S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)pent-4-ynoic acid, (2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-pentynoic acid, (2S)-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}pent-4-ynoic acid, (S)-2-(Fmoc-Amino)-4-Pentynoic Acid, 4-Pentynoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (2S)-, 4-Pentynoic acid, 2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (S)-, Fmoc-(S)-2-Propargylglycine, Fmoc-<span class="text-smallcaps">L</span>-propargylglycine, Fmoc-Pra-Oh, N-Alpha-(9-Fluorenylmethoxycarbonyl)-(S)-2-Amino-4-Pentynoic Acid, N-Alpha-(9-Fluorenylmethoxycarbonyl)-Propargylglycine, N-Alpha-(9-Fluorenylmethyloxycarbonyl)-L-Propargylglycine, Rarechem Bk Pt 0257

Beschreibung

Building block for the synthesis of precursor peptides for tritiation, and for “click chemistry”. Pra-containing peptides have been modified by 1,3-dipolar cycloaddition, e.g. with alkyl azides. Peptides containing a Pra residue and an α-azido acid have been cyclized in the presence of CuBr/Na-ascorbate via triazole formation. Educt for the synthesis of Phe-derivatives by rhodium-catalyzed [2+2+2] cycloaddition.

• Marke: Bachem

Chemische Eigenschaften

• Molekulargewicht: 335.36
• Formel: C₂₀H₁₇NO₄
• Reinheit: 99.9%
• Farbe/Form: White