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

91633-97-5

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91633-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91633-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,3 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 91633-97:
(7*9)+(6*1)+(5*6)+(4*3)+(3*3)+(2*9)+(1*7)=145
145 % 10 = 5
So 91633-97-5 is a valid CAS Registry Number.

91633-97-5Downstream Products

91633-97-5Relevant 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.

Copper-catalyzed sequential N-arylation of C-amino-NH-azoles

Nageswar Rao,Rasheed, Sk.,Vishwakarma, Ram A.,Das, Parthasarathi

supporting information, p. 12911 - 12914 (2014/12/11)

Copper(ii)-catalyzed boronic acid promoted C-N bond cross-coupling reactions have been successfully developed for sequential N-arylation of C-amino-NH-azoles. These general protocols are compatible with a variety of aryl/hetero-aryl boronic acids and provided rapid access to a diverse array of diarylaminoazole derivatives in a two-step sequence or in one-pot. This journal is

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