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L512893

Sigma-Aldrich

tert-Butyl 5-oxo-3,4-diphenyl-5,6-dihydropyridine-1(2H)-carboxylate

Synonym(s):

tert-butyl 5-oxo-3,4-diphenyl-5,6-dihydropyridine-1(2H)-carboxylate

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About This Item

Empirical Formula (Hill Notation):
C22H23NO3
Molecular Weight:
349.42
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

SMILES string

O=C1C(C2=CC=CC=C2)=C(C3=CC=CC=C3)CN(C(OC(C)(C)C)=O)C1

InChI

1S/C22H23NO3/c1-22(2,3)26-21(25)23-14-18(16-10-6-4-7-11-16)20(19(24)15-23)17-12-8-5-9-13-17/h4-13H,14-15H2,1-3H3

InChI key

OFJONGZAQBTUPW-UHFFFAOYSA-N

Application

This innovative 3-piperidinone was obtained utilizing a Ni-catalyzed, [4+2] cycloaddition developed by Louie and coworkers.

A Single Step Approach to Piperidines via Ni-Catalyzed β-Carbon Elimination

Other Notes

Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product. Buyer assumes responsibility to confirm product identity and/or purity. All sales are final.

NOTWITHSTANDING ANY CONTRARY PROVISION CONTAINED IN SIGMA-ALDRICH′S STANDARD TERMS AND CONDITIONS OF SALE OR AN AGREEMENT BETWEEN SIGMA-ALDRICH AND BUYER, SIGMA-ALDRICH SELLS THIS PRODUCT "AS-IS" AND MAKES NO REPRESENTATION OR WARRANTY WHATSOEVER WITH RESPECT TO THIS PRODUCT, INCLUDING ANY (A) WARRANTY OF MERCHANTABILITY; (B) WARRANTY OF FITNESS FOR A PARTICULAR PURPOSE; OR (C) WARRANTY AGAINST INFRINGEMENT OF INTELLECTUAL PROPERTY RIGHTS OF A THIRD PARTY; WHETHER ARISING BY LAW, COURSE OF DEALING, COURSE OF PERFORMANCE, USAGE OF TRADE OR OTHERWISE.

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pcodes

Hazard Classifications

Skin Sens. 1

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Related Content

Professor Louie's research focuses on the discovery and mechanistic understanding of new reactions catalyzed by transition metal complexes. She has developed a highly active Ni(0) catalyst that effectively mediates a variety of cycloaddition and isomerization reactions.

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