E45600
N-哌嗪甲酸乙酯
99%
别名:
1-乙氧基羰基哌嗪, 1-哌嗪羧酸乙酯
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关于此项目
经验公式（希尔记法）:
C7H14N2O2
化学文摘社编号:
分子量:
158.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-395-2
Beilstein/REAXYS Number:
125780
MDL number:
产品名称
N-哌嗪甲酸乙酯, 99%
InChI key
LNOQURRKNJKKBU-UHFFFAOYSA-N
InChI
1S/C7H14N2O2/c1-2-11-7(10)9-5-3-8-4-6-9/h8H,2-6H2,1H3
SMILES string
CCOC(=O)N1CCNCC1
assay
99%
form
liquid
refractive index
n20/D 1.477 (lit.)
bp
273 °C (lit.)
density
1.08 g/mL at 25 °C (lit.)
Quality Level
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存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Karolina Klesiewicz et al.
The Journal of antibiotics, 69(11), 825-834 (2016-03-31)
A series of 20 xanthone derivatives was synthesized and evaluated for anti-Helicobacter pylori (H. pylori) activity. Qualitative and quantitative in vitro tests using the Kirby-Bauer method (agar disc-diffusion method) were performed. The tested compounds were screened against clarithromycin- and/or metronidazole-resistant
Natalia Szkaradek et al.
Anti-cancer agents in medicinal chemistry, 19(16), 1949-1965 (2019-04-06)
Natural plant metabolites and their semisynthetic derivatives have been used for years in cancer therapy. Xanthones are oxygenated heterocyclic compounds produced as secondary metabolites by higher plants, fungi or lichens. Xanthone core may serve as a template in the synthesis
Paul J Shami et al.
Journal of medicinal chemistry, 49(14), 4356-4366 (2006-07-11)
The literature provides evidence that metabolic nitric oxide (NO) release mediates the cytotoxic activities (against human leukemia and prostate cancer xenografts in mice) of JS-K, a compound of structure R(2)N-N(O)=NO-Ar for which R(2)N is 4-(ethoxycarbonyl)piperazin-1-yl and Ar is 2,4-dinitrophenyl. Here
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