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Boc-Lys(Z)-OSu

ALDRICH/15541

Synonym: Nα-Boc-Nε-Cbz-L-lysine N-hydroxysuccinimide ester; Nα-Boc-Nε-Z-L-lysine hydroxysuccinimide ester; Nε-Z-Nα-Boc-L-lysine hydroxysuccinimide ester

CAS Number: 34404-36-9
Empirical Formula (Hill Notation): C23H31N3O8
Molecular Weight: 477.51
EC Number: 251-999-7
MDL Number: MFCD00037915
Linear Formula: C23H31N3O8
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-15541-25G 25 g
$1140.00
1/EA
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application(s) peptide synthesis
form powder
InChI 1S/C23H31N3O8/c1-23(2,3)33-22(31)25-17(20(29)34-26-18(27)12-13-19(26)28)11-7-8-14-24-21(30)32-15-16-9-5-4-6-10-16/h4-6,9-10,17H,7-8,11-15H2,1-3H3,(H,24,30)(H,25,31)/t17-/m0/s1
InChI key YWLICOCXPNQJPC-KRWDZBQOSA-N
mp 110-120 °C
optical activity [α]20/D -21.0±1.5°, c = 2% in dioxane
Quality Level 100 
reaction suitability reaction type: Boc solid-phase peptide synthesis
SMILES string CC(C)(C)OC(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)ON2C(=O)CCC2=O
storage temp. −20°C
Application: Reactant involved in:
• Cellular labeling and tumor MRI as a bimodal lipidic contrast agent
• Synthesis of improved peptide prodrugs 5-ALA for photodynamic therapy
• Design of high affinity peptide conjugates as markers for small peptide transporter PEPT1 (SLC15A1)
• Preparation of human growth hormone derivatives containing PEG groups
• Enantiodivergent asymmetric cyclization
• Solid-phase synthesis of peptide-cationic steroid conjugates for antibacterial screening
Packaging: 5, 25 g in poly bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
mp 110-120 °C
Storage Temp. −20°C
UNSPSC 12352200

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