124753
琥珀酰胺
98%
别名:
丁二酰胺
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关于此项目
线性分子式:
NH2COCH2CH2CONH2
化学文摘社编号:
分子量:
116.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-739-9
Beilstein/REAXYS Number:
1753983
MDL number:
Assay:
98%
InChI key
SNCZNSNPXMPCGN-UHFFFAOYSA-N
InChI
1S/C4H8N2O2/c5-3(7)1-2-4(6)8/h1-2H2,(H2,5,7)(H2,6,8)
SMILES string
NC(=O)CCC(N)=O
assay
98%
mp
260-265 °C (dec.) (lit.)
solubility
cold water: soluble 220 part, boiling water: soluble 9 part, alcohol: insoluble, diethyl ether: insoluble
functional group
amide
Quality Level
Application
琥珀酰胺已被用于表征来自半胱氨酸水解酶超家族的一种新型双缩脲水解酶 。在斜生栅藻和绿藻的培养基中作为氮源补充。
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
Further studies on the utilization of aspartic acid, succinamide, and asparagine by green algae.
Algeeus S.
Physiologia Plantarum, 3(4), 370-375 (1950)
Adaptable synthesis of C-glycosidic multivalent carbohydrates and succinamide-linked derivatization.
Gavin J Miller et al.
Organic letters, 12(22), 5262-5265 (2010-10-22)
A modular approach to the synthesis of trivalent C-glycosidic carbohydrates is described. The approach is illustrated employing carboxylate-terminated C-glycosidic d-mannose, d-glucose, and d-galactose derivatives with different length C1-linked spacer units and also core units with different length linker units attached.
Ozra Tabasi et al.
Colloids and surfaces. B, Biointerfaces, 98, 18-25 (2012-06-02)
The present work concerns a preliminary step in the production of anticancer drug loaded porous silicon (PSi) for targeted-drug-delivery applications. A successful procedure for the covalent attachment of folic acid, polyethylene glycol (PEG) and doxorubicin to hydrophilic mesoporous silicon layers
Olaf F A Larsen et al.
Proceedings of the National Academy of Sciences of the United States of America, 102(38), 13378-13382 (2005-09-10)
Femtosecond 2D-IR spectroscopy has been used to study the structure of a [2]rotaxane composed of a benzylic amide macrocycle that is mechanically interlocked onto a succinamide-based thread. Both the macrocycle and the thread contain carbonyl groups, and by determining the
M C Pirrung et al.
Bioorganic & medicinal chemistry letters, 10(18), 2115-2118 (2000-09-22)
A method for encoding solid-phase split/mix combinatorial libraries using the chemical shift of synthetic fluoroarenes ('F-codes') has been developed. They have wide chemical shift dispersion and are detectable at the sub-micromol level. 19F NMR is used for decoding. Nine fluoroarenes
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