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重要文件

198064

Sigma-Aldrich

4-氨基-1-哌啶甲酸乙酯

96%

同義詞:

1-Carbethoxy-4-aminopiperidine

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About This Item

經驗公式(希爾表示法):
C8H16N2O2
CAS號碼:
分子量::
172.22
Beilstein:
388597
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

96%

形狀

liquid

折射率

n20/D 1.483 (lit.)

密度

1.004 g/mL at 25 °C (lit.)

SMILES 字串

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 密鑰

GQQQULCEHJQUJT-UHFFFAOYSA-N

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應用

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

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

172.4 °F - closed cup

閃點(°C)

78 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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分析證明 (COA)

Lot/Batch Number

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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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