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ethyl 4-((4-bromophenyl)(methyl)amino)-3-oxobutanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1364822-75-2

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1364822-75-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1364822-75-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,4,8,2 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1364822-75:
(9*1)+(8*3)+(7*6)+(6*4)+(5*8)+(4*2)+(3*2)+(2*7)+(1*5)=172
172 % 10 = 2
So 1364822-75-2 is a valid CAS Registry Number.

1364822-75-2Relevant academic research and scientific papers

Direct amination of γ-Halo-β-ketoesters with anilines

Zhang, Yinan,Silverman, Richard B.

, p. 3462 - 3467 (2012)

The direct amination of α-haloacetoacetates with anilines is described. Compared to existing methods, this simple protocol provides an attractive strategy to prepare diverse γ-anilino-β-ketoesters in one step. Good to excellent yields of the amination products were obtained under robust conditions, providing versatile and useful scaffolds.

Arylazanylpyrazolone derivatives as inhibitors of mutant superoxide dismutase 1 dependent protein aggregation for the treatment of amyotrophic lateral sclerosis

Zhang, Yinan,Benmohamed, Radhia,Huang, He,Chen, Tian,Voisine, Cindy,Morimoto, Richard I.,Kirsch, Donald R.,Silverman, Richard B.

, p. 2665 - 2675 (2013/05/22)

The arylsulfanylpyrazolone and aryloxanylpyrazolone scaffolds previously were reported to inhibit Cu/Zn superoxide dismutase 1 dependent protein aggregation and to extend survival in the ALS mouse model. However, further evaluation of these compounds indicated weak pharmacokinetic properties and a relatively low maximum tolerated dose. On the basis of an ADME analysis, a new series of compounds, the arylazanylpyrazolones, has been synthesized, and structure-activity relationships were determined. The SAR results showed that the pyrazolone ring is critical to cellular protection. The NMR, IR, and computational analyses suggest that phenol-type tautomers of the pyrazolone ring are the active pharmacophore with the arylazanylpyrazolone analogues. A comparison of experimental and calculated IR spectra is shown to be a valuable method to identify the predominant tautomer.

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