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153737

Ethyl 4-oxo-1-piperidinecarboxylate

98%

Synonym(s):

1-Carbethoxy-4-piperidone, 1-Ethoxycarbonyl-4-piperidone

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About This Item

Empirical Formula (Hill Notation):
C8H13NO3
CAS Number:
29976-53-2
Molecular Weight:
171.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24849369
EC Number:
249-984-5
Beilstein/REAXYS Number:
640967
MDL number:
MFCD00006188
Assay:
98%

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InChI key

LUBGFMZTGFXIIN-UHFFFAOYSA-N

InChI

1S/C8H13NO3/c1-2-12-8(11)9-5-3-7(10)4-6-9/h2-6H2,1H3

SMILES string

CCOC(=O)N1CCC(=O)CC1

assay

98%

Quality Level

100

density

1.135 g/mL at 25 °C (lit.)

functional group

ketone

refractive index

n20/D 1.475 (lit.)

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This Item
198064130036678953
Ethyl 4-oxo-1-piperidinecarboxylate 98%

Sigma-Aldrich

153737

Ethyl 4-oxo-1-piperidinecarboxylate

Ethyl 4-amino-1-piperidinecarboxylate 96%

Sigma-Aldrich

198064

Ethyl 4-amino-1-piperidinecarboxylate

N-Methyl-4-piperidone 97%

Sigma-Aldrich

130036

N-Methyl-4-piperidone

4-(1-Piperidinyl)benzaldehyde 97%

Sigma-Aldrich

678953

4-(1-Piperidinyl)benzaldehyde

assay

98%

assay

96%

assay

97%

assay

97%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

density

1.135 g/mL at 25 °C (lit.)

density

1.004 g/mL at 25 °C (lit.)

density

0.92 g/mL at 25 °C (lit.)

density

-

refractive index

n20/D 1.475 (lit.)

refractive index

n20/D 1.483 (lit.)

refractive index

-

refractive index

-

functional group

ketone

functional group

-

functional group

ketone

functional group

aldehyde

Application

Ethyl 4-oxo-1-piperidinecarboxylate (1-carbethoxy-4-piperidone) was used to prepare tertiary alcohols[1].

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

188.6 °F

flash_point_c

87 °C

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificates of Analysis (COA)

Lot/Batch Number
S10696
02202AH
08401HE
06131EE
08608PW

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Eric Gundersen et al.
Bioorganic & medicinal chemistry letters, 15(7), 1891-1894 (2005-03-23)
Alzheimer's disease (AD) is a debilitating disease widely thought to be associated with the accumulation of beta amyloid (Abeta) in the brain. Inhibition of gamma-secretase, one of the enzymes responsible for Abeta production, may be a useful strategy for the

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