Key Documents

View All Documentation

464643

1-Z-4-Piperidone

Name: 1-Z-4-Piperidone
Brand: ALDRICH

99%

Synonym(s):

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

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):

C₁₃H₁₅NO₃

CAS Number:

19099-93-5

Molecular Weight:

233.26

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24870202

MDL number:

MFCD00673144

Beilstein/REAXYS Number:

1533716

Assay:

99%

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

assay

99%

refractive index

n20/D 1.542 (lit.)

bp

114-140 °C/0.25 mmHg (lit.)

density

1.172 g/mL at 25 °C (lit.)

functional group

ketone, phenyl

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

Description

Still not finding the right product?

Explore all of our products under 1-Z-4-Piperidone

pictograms

GHS07

signalword

Warning

hcodes

H302,H412

pcodes

P264 - P270 - P273 - P301 + P312 - P501

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, multi-purpose combination respirator cartridge (US)

Regulatory Information

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Articles

Knoevenagel Condensation Reaction

Knoevenagel Condensation is an organic reaction named after Emil Knoevenagel. It is a classic C-C bond formation reaction and a modification of the Aldol Condensation.

Tetrahedron Letters, 42, 6943-6943 (2001)

Hydrogen-bond-promoted hetero-Diels-Alder reactions of unactivated ketones.

Yong Huang et al.

Journal of the American Chemical Society, 124(33), 9662-9663 (2002-08-15)

We report the first examples of hydrogen-bond-promoted acceleration of hetero-Diels-Alder reactions and the use of such catalysis for the hetero-Diels-Alder reactions of simple, unactivated ketones. Several spiro-fused dihydropyans were synthesized in good yields using this procedure. This activation protocol represents

Design and pharmacology of N-[(3R)-1,2,3,4-tetrahydroisoquinolinium- 3-ylcarbonyl]-(1R)-1-(4-chlorobenzyl)- 2-[4-cyclohexyl-4-(1H-1,2,4-triazol- 1-ylmethyl)piperidin-1-yl]-2-oxoethylamine (1), a potent, selective, melanocortin subtype-4 receptor agonist.

Iyassu K Sebhat et al.

Journal of medicinal chemistry, 45(21), 4589-4593 (2002-10-04)

Synthetic and natural peptides that act as nonselective melanocortin receptor agonists have been found to be anorexigenic and to stimulate erectile activity. We report the design and development of 1, a potent, selective (1184-fold vs MC3R, 350-fold vs MC5R), small-molecule

View All Related Papers

Global Trade Item Number

SKU	GTIN
464643-25ML	04061838128010
464643-100ML	04061838128003
464643-5ML	04061838128027