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E45600

Sigma-Aldrich

Ethyl 1-piperazinecarboxylate

99%

Synonym(s):

1-Ethoxycarbonylpiperazine, Piperazine-1-carboxylic acid ethyl ester

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About This Item

Empirical Formula (Hill Notation):
C7H14N2O2
CAS Number:
120-43-4
Molecular Weight:
158.20
Beilstein/REAXYS Number:
125780
EC Number:
204-395-2
MDL number:
MFCD00005964
UNSPSC Code:
12352100
PubChem Substance ID:
24894563
NACRES:
NA.22

Quality Level

100

assay

99%

form

liquid

refractive index

n20/D 1.477 (lit.)

bp

273 °C (lit.)

density

1.08 g/mL at 25 °C (lit.)

SMILES string

CCOC(=O)N1CCNCC1

InChI

1S/C7H14N2O2/c1-2-11-7(10)9-5-3-8-4-6-9/h8H,2-6H2,1H3

InChI key

LNOQURRKNJKKBU-UHFFFAOYSA-N

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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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