推荐产品
化驗
97%
mp
153-156 °C (lit.)
官能基
amide
carboxylic acid
SMILES 字串
NC(=O)CCC(O)=O
InChI
1S/C4H7NO3/c5-3(6)1-2-4(7)8/h1-2H2,(H2,5,6)(H,7,8)
InChI 密鑰
JDVPQXZIJDEHAN-UHFFFAOYSA-N
一般說明
琥珀酰胺酸可形成双核铕络合物。它可与K2PtCl4形成混合价铂蓝。
訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Structure and photophysical properties of europium complexes of succinamic acid and 1, 10-phenanthroline.
Polyhedron, 22(2), 323-330 (2003)
Synthesis, binding sites, and spectroscopic characterizations of succinamic acid and succinimide platinum blues.
Journal of the American Chemical Society, 106(5), 1300-1303 (1984)
Scientific reports, 10(1), 16430-16430 (2020-10-04)
The hair bundle of cochlear hair cells is the site of auditory mechanoelectrical transduction. It is formed by three rows of stiff microvilli-like protrusions of graduated heights, the short, middle-sized, and tall stereocilia. In developing and mature sensory hair cells
Cell chemical biology, 24(12), 1467-1478 (2017-10-17)
Fucosylation is a glycan modification critically involved in cancer and inflammation. Although potent fucosylation inhibitors are useful for basic and clinical research, only a few inhibitors have been developed. Here, we focus on a fucose analog with an alkyne group
Frontiers in microbiology, 8, 435-435 (2017-04-04)
Commensal non-toxigenic
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.
联系技术服务部门