登录 查看组织和合同定价。
选择尺寸
变更视图
关于此项目
经验公式(希尔记法):
C9H8N2O7
化学文摘社编号:
分子量:
256.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
EC Number:
277-730-3
MDL number:
Beilstein/REAXYS Number:
1499137
产品名称
N,N′-二琥珀酰亚胺碳酸酯, purum, ≥95.0% (NMR)
grade
purum
Quality Level
assay
≥95.0% (NMR)
form
powder
reaction suitability
reaction type: Carbonylations
impurities
~3% N-hydroxysuccinimide (NMR)
mp
190 °C (dec.) (lit.)
application(s)
peptide synthesis
functional group
imide
storage temp.
−20°C
SMILES string
O=C1CCC(=O)N1OC(=O)ON2C(=O)CCC2=O
InChI
1S/C9H8N2O7/c12-5-1-2-6(13)10(5)17-9(16)18-11-7(14)3-4-8(11)15/h1-4H2
InChI key
PFYXSUNOLOJMDX-UHFFFAOYSA-N
Application
N,N′-碳酸二琥珀酰亚胺基酯(DSC)可用于:
它可用于:
- 通过烷氧基羰基化反应,合成来自伯和空间受阻的仲醇的各种氨基甲酸酯衍生物。
- 由4-羟基甲基聚苯乙烯和4-羟基甲基-3-硝基苯甲酰胺树脂,经羟基官能团合成活性碳酸酯树脂。
- 氮杂-甘氨酰二肽,用于制备多种氮杂肽的一种重要中间体。
它可用于:
- 5-(6-(叠氮甲基)烟酰胺基)戊酸的两步制备中,其是一种铜螯合的吡啶甲基叠氮化物衍生物。
- 激活半抗原γ-羟基苯基丁酮(HPBZ)的羟基,从而使HPBZ可以有效地与人血清白蛋白(HSA)-免疫原结合形成半抗原-蛋白质结合物。
Other Notes
用于制备 N-保护性氨基酸和其他酸的 N-琥珀酰亚胺基酯的简便试剂;活化碳酸盐,例如合成尿素和氨基甲酸盐;将配体偶联至蛋白质(通过赖氨酸)。
Still not finding the right product?
Explore all of our products under N,N′-二琥珀酰亚胺碳酸酯
signalword
Warning
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
hcodes
Hazard Classifications
Acute Tox. 4 Oral
T. Kokubo et al.
Journal of the American Chemical Society, 109, 606-606 (1987)
M Morpurgo et al.
Journal of biochemical and biophysical methods, 38(1), 17-28 (1999-03-17)
Ligands containing amino or hydroxyl groups were converted to their corresponding activated N-hydroxysuccinimidyl carbamate and carbonate by reaction with disuccinimidyl carbonate (DSC). The latter reagents can be used for the group-specific modification of primary amines as an alternative to the
A.K. Ghosh et al.
Tetrahedron Letters, 33, 2781-2781 (1992)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 49617-250MG | 04061832416083 |
| 43720-25G | 04061833417072 |
| 43720-5G | 04061833348444 |
