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Predict NMR spectrum
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InChI: |
1S/C25H28N2O6/c1-2-15-32-24(30)26-14-8-7-13-22(23(28)29)27-25(31)33-16-21-19-11-5-3-9-17(19)18-10-4-6-12-20(18)21/h2-6,9-12,21-22H,1,7-8,13-16H2,(H,26,30)(H,27,31)(H,28,29)/t22-/m0/s1 |
InChIKey: |
OJBNDXHENJDCBA-QFIPXVFZSA-N |
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H donor: |
3 |
H acceptor: |
8 |
Rotatable bond: |
13 |
Stereocenter: |
1 |
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cLogP: |
4.003 |
cLogS: |
-5.904 |
Polar surface: |
113.96 |
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Supplier
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Description
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Reference
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bocsci
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Nα-Fmoc-Nε-allyloxycarbonyl-L-lysine, ≥ 99.5% (Chiral HPLC)
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amadischem
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Fmoc-Lys(Alloc)-OH, 98%
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advtechind
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fmoc-lys(aloc)-oh
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on request |
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10 CARTRIDGES |
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on request |
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1 G |
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on request |
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5 G |
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leapchem
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fmoc-lys(alloc)-oh
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leapchem
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fmoc-lys(aloc)-oh
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alfa-chemistry
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Orthogonally-protected building block for the synthesis of branched and cyclic peptides and peptides modified at the Lys side chain by Fmoc SPPS. The Alloc group can be selectively removed in the presence of standard Fmoc- and t-butyl-based protecting groups by treatment with Pd(Ph3P)4/CHCl3/AcOH/NMM.
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leapchem
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fmoc-lys(alloc)-oh, 98%
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capotchem
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Fmoc-Lys(Alloc)-OH, 98%(Min,HPLC)
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chemieliva
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Fmoc-L-Lys(Alloc)-OH, 98%
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chemcube
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(S)-1-(9H-fluoren-9-yl)-3,11-dioxo-2,12-dioxa-4,10-diazapentadec-14-ene-5-carboxylic acid |
Fmoc-Lys(Alloc)-OH |
N-alpha-Fmoc-N-epsilon-allyloxycarbonyl-L-lysine |
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carbonesci
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Fmoc-lys(alloc)-OH, 98%
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oakwood
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chemtour
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Fmoc-Lys(Alloc)-OH, 99%
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glbiochem
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(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-6-{[(prop-2-en-1-yloxy)carbonyl]amino}hexanoic acid, 98%
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cslabs
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Fmoc-Lys(Alloc)-OH
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bocsci
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Nα-Fmoc-Nε-allyloxycarbonyl-L-lysine, ≥ 99.5% (Chiral HPLC)
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aceschem
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Fmoc-Lys(Alloc)-OH, 98%NLT
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chempur
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Fmoc-Lys(Alloc)-OH/ 98%
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lingruichem
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FMOC-LYS(ALOC)-OH
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activate-scientific
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N2-Fmoc-N6-[(allyloxy)carbonyl]-L-lysine, 97% ee
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