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Fmoc-L-Lys(Alloc)-OH
Predict NMR spectrum
RN: 
146982-27-6
MF: 
C25H28N2O6
MW: 
452.50712
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
H donor:  3
H acceptor:  8
Rotatable bond:  13
Stereocenter:  1
cLogP:  4.003
cLogS:  -5.904
Polar surface:  113.96
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  Supplier     Description     Reference  
bocsci Nα-Fmoc-Nε-allyloxycarbonyl-L-lysine, ≥ 99.5% (Chiral HPLC)
on request
capotchem Fmoc-Lys(Alloc)-OH, 98%(Min,HPLC)
1kg
5kg
25kg
100kg
200kg
tons
amadischem Fmoc-Lys(Alloc)-OH, 98%
Bulk, semi-bulk
advtechind fmoc-lys(aloc)-oh
10 CARTRIDGES
1 G
5 G
leapchem fmoc-lys(aloc)-oh
on request
leapchem fmoc-lys(alloc)-oh
on request
alfa-chemistry 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.
1g
5g
10g
25g
100g
250g
leapchem fmoc-lys(alloc)-oh, 98%
on request
aifchem Fmoc-Lys(Alloc)-OH, 98%
100g
500g
cm-finechemicals N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N6-[(2-propen-1-yloxy)carbonyl]-L-lysine
Pilot
Commercial
chemcube
(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
 , >98%
on request
advtechind fmoc-lys(alloc)-oh 98.0%
INQUIRY
lingruichem FMOC-LYS(ALOC)-OH
on request
lingruichem FMOC-LYS(ALOC)-OH
on request
lingruichem Fmoc-Lys(Alloc)-OH
on request
carbonesci Fmoc-lys(alloc)-OH, 98%
on request
lingruichem FMOC-LYS(ALOC)-OH
on request
oakwood
Fmoc-Lys(Alloc)-OH
 , 98%
250mg
1g
5g
yuansu-reagent FMOC-LYS(ALOC)-OH
qcsrm Semaglutide Impurity 64

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