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Merck
CN

13635

1-Z-4-Piperidone

purum, ≥95.0% (HPLC)

Synonym(s):

1-(Benzyloxycarbonyl)-4-piperidinone, 1-Cbz-4-Piperidone, Benzyl 4-oxo-1-piperidinecarboxylate

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About This Item

Empirical Formula (Hill Notation):
C13H15NO3
CAS Number:
19099-93-5
Molecular Weight:
233.26
Beilstein/REAXYS Number:
1533716
PubChem Substance ID:
329750051
UNSPSC Code:
12352100
MDL number:
MFCD00673144
Assay:
≥95.0% (HPLC)
Form:
solid

Key Documents

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SMILES string

O=C1CCN(CC1)C(=O)OCc2ccccc2

InChI

1S/C13H15NO3/c15-12-6-8-14(9-7-12)13(16)17-10-11-4-2-1-3-5-11/h1-5H,6-10H2

InChI key

VZOVOHRDLOYBJX-UHFFFAOYSA-N

grade

purum

assay

≥95.0% (HPLC)

form

solid

Quality Level

100

bp

114-140 °C/0.25 mmHg (lit.)

density

1.172 g/mL at 25 °C (lit.)

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General description

1-Z-4-Piperidone is the starting material in biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol condensation reactions.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H412

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves

Regulatory Information

危险化学品
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Biheteroaromatic diphosphine oxides-catalyzed stereoselective direct aldol reactions.
Rossi S, et al.
Tetrahedron, 67(1), 158-166 (2011)
Svetlana Paskaš et al.
Molecular carcinogenesis, 58(8), 1362-1375 (2019-04-19)
The main focus of this study is exploring the effect and mechanism of two HIV-protease inhibitors: Ritonavir and Ritonavir-nitric oxide (Ritonavir-NO) on in vitro growth of melanoma cell lines. NO modification significantly improved the antitumor potential of Ritonavir, as the

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