15385
Boc-Ala-OSu
别名:
Boc-L-丙氨酸-N-丁二酰亚胺酯, Boc-L-丙氨酸丁二酰亚胺酯
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C12H18N2O6
化学文摘社编号:
分子量:
286.28
UNSPSC Code:
12352202
NACRES:
NA.22
PubChem Substance ID:
EC Number:
222-229-7
Beilstein/REAXYS Number:
3560476
MDL number:
InChI key
COMUWNFVTWKSDT-ZETCQYMHSA-N
InChI
1S/C12H18N2O6/c1-7(13-11(18)19-12(2,3)4)10(17)20-14-8(15)5-6-9(14)16/h7H,5-6H2,1-4H3,(H,13,18)/t7-/m0/s1
SMILES string
C[C@H](NC(=O)OC(C)(C)C)C(=O)ON1C(=O)CCC1=O
form
solid
optical activity
[α]20/D −52±3.5°, c = 2.5% in dioxane
reaction suitability
reaction type: Boc solid-phase peptide synthesis
mp
161-165 °C
application(s)
peptide synthesis
storage temp.
−20°C
Application
Reactant involved in synthesis of:
- Muramyldipeptide analogs via solid-phase synthesis
- Microcin C analogs for use as antibacterials
- Lipid I and nucleoside diphosphate peptide derivatives via N-methylimidazolium chloride catalyzed coupling
- N-Protected dipeptide acids
- Free and peptide-bound glycated amino acids for studies of interactions with human Caco-2 interstinal epithelial cell apical membrane transport proteins
- 7-Substituted camptothecin conjugates with RGD-peptides as avβ3 integrin ligands
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持