N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[[(2-propyn-1-yloxy)carbonyl]amino]-L-phenylalanine

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N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[[(2-propyn-1-yloxy)carbonyl]amino]-L-phenylalanine Basic information
Product Name:N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[[(2-propyn-1-yloxy)carbonyl]amino]-L-phenylalanine
Synonyms:N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[[(2-propyn-1-yloxy)carbonyl]amino]-L-phenylalanine
CAS:2576508-07-9
MF:C28H24N2O6
MW:484.5
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Mol File:2576508-07-9.mol
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[[(2-propyn-1-yloxy)carbonyl]amino]-L-phenylalanine Structure
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[[(2-propyn-1-yloxy)carbonyl]amino]-L-phenylalanine Chemical Properties
Boiling point 678.2±55.0 °C(Predicted)
density 1.347±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)
pka3.78±0.10(Predicted)
Safety Information
MSDS Information
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[[(2-propyn-1-yloxy)carbonyl]amino]-L-phenylalanine Usage And Synthesis
UsesFmoc-L-Phe(4-NH-Poc)-OH is a click chemistry reagent containing an azide group. Used as an orthogonally protected building block in solid-phase peptide synthesis. Poc-group can be further modified using Click-chemistry[1].
References[1] Jiang X, et al. Recent applications of click chemistry in drug discovery. Expert Opin Drug Discov. 2019 Aug;14(8):779-789. DOI:10.1080/17460441.2019.1614910
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[[(2-propyn-1-yloxy)carbonyl]amino]-L-phenylalanine Preparation Products And Raw materials
Tag:N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[[(2-propyn-1-yloxy)carbonyl]amino]-L-phenylalanine(2576508-07-9) Related Product Information
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