225827
N,N′-二琥珀酰亚胺碳酸酯
≥95%, for peptide synthesis
别名:
N-琥珀酰氨基碳酸酯, DSC, 二(N-琥珀酰亚胺基)碳酸酯
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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:
12352108
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, ≥95%
InChI key
PFYXSUNOLOJMDX-UHFFFAOYSA-N
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
SMILES string
O=C1CCC(=O)N1OC(=O)ON2C(=O)CCC2=O
assay
≥95%
form
powder or crystals
reaction suitability
reaction type: Carbonylations
mp
190 °C (dec.) (lit.)
application(s)
peptide synthesis
functional group
imide
storage temp.
2-8°C
Quality Level
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Application
N，N′-碳酸二琥珀酰亚胺酯可用于：
- 作为活化剂，通过后官能化将聚合物刷与伯胺进行偶联，从而用于改变其反应模式。
- 作为多种伯醇和空间受阻的仲醇的烷氧羰基化试剂，它还可以用于合成结构上不同的氨基甲酸酯。
- 作为合成硫代磷脂的偶联剂，通常可用于将生物膜固定在金表面。
General description
N，N′-碳酸二琥珀酰亚胺酯可用于通过HPLC对氨基化合物进行测定。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - STOT RE 2 Oral
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
Tetrahedron Letters, 33, 2781-2781 (1992)
N,N?-Disuccinimidyl carbonate as a coupling agent in the synthesis of thiophospholipids used for anchoring biomembranes to gold surfaces
Boden N, et al.
Tetrahedron, 54(38), 11537-11548 (1998)
Chang-Juan Tao et al.
Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology, 115(3), 407-411 (2015-05-31)
To assess whether consensus guideline-based atlas-based auto-segmentation (ABAS) reduces interobserver variation and improves dosimetric parameter consistency for organs at risk (OARs) in nasopharyngeal carcinoma (NPC). Eight radiation oncologists from 8 institutes contoured 20 OARs on planning CT images of 16
N, N?-Disuccinimidyl Carbonate: A Useful Reagent for Alkoxycarbonylation of Amines
Ghosh KA, et al.
Tetrahedron Letters, 33(20), 2781-2781 (1992)
Reactive patterning via post-functionalization of polymer brushes utilizing disuccinimidyl carbonate activation to couple primary amines
Diamanti S, et al.
Polymer, 49(17), 3770-3779 (2008)
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