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15435

Sigma-Aldrich

Boc-Lys(Fmoc)-OH

≥99.0% (sum of enantiomers, TLC)

Synonym(s):

Nα-Boc-Nε-Fmoc-L-lysine

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About This Item

Empirical Formula (Hill Notation):
C26H32N2O6
CAS Number:
Molecular Weight:
468.54
Beilstein/REAXYS Number:
3576584
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26

assay

≥99.0% (sum of enantiomers, TLC)

form

solid

optical activity

[α]20/D +3.3±0.5°, c = 1% in ethyl acetate

reaction suitability

reaction type: Boc solid-phase peptide synthesis

application(s)

peptide synthesis

functional group

Boc
Fmoc

storage temp.

2-8°C

SMILES string

CC(C)(C)OC(=O)N[C@@H](CCCCNC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C26H32N2O6/c1-26(2,3)34-25(32)28-22(23(29)30)14-8-9-15-27-24(31)33-16-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h4-7,10-13,21-22H,8-9,14-16H2,1-3H3,(H,27,31)(H,28,32)(H,29,30)/t22-/m0/s1

InChI key

JYEVQYFWINBXJU-QFIPXVFZSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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