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198064

Sigma-Aldrich

Ethyl 4-amino-1-piperidinecarboxylate

96%

Synonym(s):

1-Carbethoxy-4-aminopiperidine

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About This Item

Empirical Formula (Hill Notation):
C8H16N2O2
CAS Number:
58859-46-4
Molecular Weight:
172.22
Beilstein/REAXYS Number:
388597
EC Number:
261-472-3
MDL number:
MFCD00006484
UNSPSC Code:
12352100
PubChem Substance ID:
24851859
NACRES:
NA.22

Quality Level

100

assay

96%

form

liquid

refractive index

n20/D 1.483 (lit.)

density

1.004 g/mL at 25 °C (lit.)

SMILES string

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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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

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

wgk_germany

WGK 3

flash_point_f

172.4 °F

flash_point_c

78 °C

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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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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