| Identification | Back Directory | [Name]
Fmoc-Lys(N3)-OH | [CAS]
159610-89-6 | [Synonyms]
FMoc-Lys(N2)-OH
Fmoc-Lys(N3)-OH
Fmoc-L-Lys(N3)-OH
FMoc-L-azidolysine
FMoc-e-azido-Nle-OH
Fmoc-ε-azido-Nle-OH
Nα-Fmoc-Nε-azide-L-Lysine
6-Azido-N-Fmoc-L-norleucine
(2S)-N-FMoc-6-azido--Hexanoic acid
(2S)-N-FMoc-5-azido- hexanoic acid
(9H-Fluoren-9-yl)MethOxy]Carbonyl Lys(N3)-OH
Nα-Fmoc-Nε-azide-L-Lysine≥ 99.9% (HPLC, Chiral purity)
N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-diazo-L-lysine
6-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-norleucine
L-Norleucine, 6-azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
(2S)-6-azido-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-azidohexanoic acid
6-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-norleucine | [Molecular Formula]
C21H22N4O4 | [MDL Number]
MFCD13182319 | [MOL File]
159610-89-6.mol | [Molecular Weight]
394.42 |
| Hazard Information | Back Directory | [Chemical Properties]
White to off-white crystalline powder | [Uses]
The side chain azido (N3) group is stable in trifluoroacetic acid or piperidine. It can be readily converted to amine and to synthesis side chain modified peptides and proteins by Solid Phase Peptide Synthesis (SPPS) methodology. |
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Shanghai GL Peptide Ltd. Gold
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http://m.is0513.com/supplier/10480342/ |
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