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About This Item
经验公式（希尔记法）:
C8H16N2O2
CAS号:
分子量:
172.22
Beilstein:
388597
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
质量水平
方案
96%
表单
liquid
折射率
n20/D 1.483 (lit.)
密度
1.004 g/mL at 25 °C (lit.)
SMILES字符串
CCOC(=O)N1CCC(N)CC1
InChI
1S/C8H16N2O2/c1-2-12-8(11)10-5-3-7(9)4-6-10/h7H,2-6,9H2,1H3
InChI key
GQQQULCEHJQUJT-UHFFFAOYSA-N
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应用
Ethyl 4-amino-1-piperidinecarboxylate (1-Carbethoxy-4-aminopiperidine) was used in the synthesis of quinolin-2(1H )-one derivatives.
Reactant for synthesis of:
Milrinone analogs to analyze effects on intracellular calcium increase in cardiac cells
Tetrahydronaphthalene derivatives
Quorum sensing modulators
Selective anti-Helicobacter pylori activity molecules
Orally active M1 mAChR agonists
Aza derivatives of phytoalexin for antibacterial activity
Milrinone analogs to analyze effects on intracellular calcium increase in cardiac cells
Tetrahydronaphthalene derivatives
Quorum sensing modulators
Selective anti-Helicobacter pylori activity molecules
Orally active M1 mAChR agonists
Aza derivatives of phytoalexin for antibacterial activity
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
172.4 °F - closed cup
闪点(°C)
78 °C - closed cup
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
Christopher Blackburn et al.
Bioorganic & medicinal chemistry letters, 16(10), 2621-2627 (2006-03-10)
Several potent, functionally active MCHr1 antagonists derived from quinolin-2(1H)-ones and quinazoline-2(1H)-ones have been synthesized and evaluated. Pyridylmethyl substitution at the quinolone 1-position results in derivatives with low-nM binding potency and good selectivity with respect to hERG binding.
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