15541
Boc-Lys(Z)-OSu
别名:
Nα-Boc-Nε-Cbz-L-赖氨酸 N-羟基琥珀酰亚胺酯, Nα-Boc-Nε-Z-L-赖氨酸羟基琥珀酰亚胺酯, Nε-苄氧羰基-Nα-叔丁氧羰基-L-赖氨酸羟基琥珀酰亚胺酯
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选择尺寸
关于此项目
经验公式（希尔记法）:
C23H31N3O8
化学文摘社编号:
分子量:
477.51
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
251-999-7
MDL number:
Beilstein/REAXYS Number:
1559393
InChI key
YWLICOCXPNQJPC-KRWDZBQOSA-N
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
SMILES string
CC(C)(C)OC(=O)N[C@@H](CCCCNC(=O)OCc1ccccc1)C(=O)ON2C(=O)CCC2=O
form
powder
optical activity
[α]20/D -21.0±1.5°, c = 2% in dioxane
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
110-120 °C
application(s)
peptide synthesis
storage temp.
−20°C
Quality Level
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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
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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