所有图片(2)
About This Item
经验公式（希尔记法）:
C4H8N2O4
CAS号:
分子量:
148.12
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
表单
powder
反应适用性
reaction type: solution phase peptide synthesis
颜色
white
应用
peptide synthesis
SMILES字符串
NC(C(N)C(O)=O)C(O)=O
InChI
1S/C4H8N2O4/c5-1(3(7)8)2(6)4(9)10/h1-2H,5-6H2,(H,7,8)(H,9,10)/t1-,2+
InChI key
PGNYNCTUBKSHHL-XIXRPRMCSA-N
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警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Kirsten Zeitler et al.
The Journal of organic chemistry, 69(18), 6134-6136 (2004-09-18)
Homogeneous, Rh-catalyzed hydrogenation of heteromeric olefinic glycine dimers presents an efficient route to diastereomerically pure, orthogonally protected diaminosuccinic acid derivatives depending on the double bond geometry of the starting material. The products were obtained as racemates.
A Rinaldi et al.
European journal of biochemistry, 117(3), 635-638 (1981-07-01)
meso-Diaminosuccinic acid, a natural antagonist of aspartic acid, is a good substrate for beef kidney D-aspartate oxidase. The oxygen consumption and the ammonia production are in good agreement with the stoichiometry of a typical oxidative deamination. The deamination involves only
C Riemer et al.
The journal of peptide research : official journal of the American Peptide Society, 63(3), 196-199 (2004-03-31)
The stereoselective synthesis of orthogonally protected 3-azido aspartic acid derivatives is described. The convenience of their application as 2,3-diaminosuccinic acid in peptide chemistry was demonstrated by the incorporation of the nonproteinogenic diamino diacid as a cystine-substitute into the core structure
J E Turner et al.
Basic life sciences, 63, 155-166 (1994-01-01)
Detailed Monte Carlo calculations provide a powerful tool for understanding mechanisms of radiation damage to biological molecules irradiated in aqueous solution. This paper describes the computer codes, OREC and RADLYS, which have been developed for this purpose over a number
Yoshito Kawasaki et al.
Journal of chromatography. A, 1160(1-2), 246-253 (2007-06-08)
The advanced Marfey's method consists of a chromatography technique for the separation of amino acids into each enantiomer by derivatization with 1-fluoro-2,4-dinitrophenyl-5-L-leucinamide (L-FDLA), and a detection method using liquid chromatography/mass spectrometry (LC/MS) which can determine the non-empirically the absolute configuration
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