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经验公式(希尔记法):
C8H16N2O2
化学文摘社编号:
分子量:
172.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
261-472-3
Beilstein/REAXYS Number:
388597
MDL number:
产品名称
4-氨基-1-哌啶甲酸乙酯, 96%
InChI key
GQQQULCEHJQUJT-UHFFFAOYSA-N
InChI
1S/C8H16N2O2/c1-2-12-8(11)10-5-3-7(9)4-6-10/h7H,2-6,9H2,1H3
SMILES string
CCOC(=O)N1CCC(N)CC1
assay
96%
form
liquid
refractive index
n20/D 1.483 (lit.)
density
1.004 g/mL at 25 °C (lit.)
Quality Level
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Application
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
172.4 °F - closed cup
flash_point_c
78 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
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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