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1H-Pyrazol-5-amine, 1-(3-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16459-43-1

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16459-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16459-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,5 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16459-43:
(7*1)+(6*6)+(5*4)+(4*5)+(3*9)+(2*4)+(1*3)=121
121 % 10 = 1
So 16459-43-1 is a valid CAS Registry Number.

16459-43-1Downstream Products

16459-43-1Relevant academic research and scientific papers

Copper(I)/Copper(II)-Assisted Tandem Catalysis: The Case Study of Ullmann/Chan-Evans-Lam N1,N3-Diarylation of 3-Aminopyrazole

Beyer, Astrid,Castanheiro, Thomas,Busca, Patricia,Prestat, Guillaume

, p. 2433 - 2436 (2015/08/24)

Unprecedented CuI/CuII-assisted tandem catalysis allowing an Ullmann/Chan-Evans-Lam sequence was achieved. This three-component, one-pot reaction triggered by a change in the oxidation state of the metal leads to the selective N1,N3-diarylation of 3-aminopyrazole. This new method should be a valuable tool for small-molecule drug discovery that requires suitable regio- and/or chemoselective strategies for the N-arylation of nitrogen-containing heterocycles. Tandem power: The first assisted tandem copper-catalyzed process, triggered by a change in the oxidation state of the metal, is developed to allow a one-pot Ullman/Chan-Evans-Lam sequence leading to the selective N1,N3-diarylation of 3-aminopyrazole.

HETEROCYCLIC DERIVATIVES AS IAP BINDING COMPOUNDS

-

, (2010/01/12)

The present invention relates to compounds of formula (I), or pharmaceutically acceptable salts, solvates thereof, that bind to Inhibitor of Apoptosis Proteins (IAPs). The compounds of the invention may be used as diagnostic and therapeutic agents in the

Inhibitors of IAP

-

Page/Page column 60, (2010/02/15)

The invention provides novel inhibitors of IAP that are useful as therapeutic agents for treating malignancies where the compounds have the general formula I: wherein X, Y, A, R1, R2, R3, R4, R4′, R5, R5′, R6 and R6′ are as described herein.

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