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1018075-52-9

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1018075-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1018075-52-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,8,0,7 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1018075-52:
(9*1)+(8*0)+(7*1)+(6*8)+(5*0)+(4*7)+(3*5)+(2*5)+(1*2)=119
119 % 10 = 9
So 1018075-52-9 is a valid CAS Registry Number.

1018075-52-9Downstream Products

1018075-52-9Relevant academic research and scientific papers

Synthesis of new 4-methyl-2-(4-pyridyl)-1,2,3,4-tetrahydroquinolines as potent antifungal compounds

Vargas Méndez, Leonor Y.,Zacchinob, Susana A.,Kouznetsov, Vladimir V.

experimental part, p. 105 - 111 (2010/08/22)

Synthesis, spectral characterization and biological results of new series of 2-(4-pyridyl)- 1,2,3,4-tetrahydroquinolines and their closer precursors, -N-aryl-N-[1-(4-pyridyl)but-3-enyl] amines are reported. It was found that both g-pyridyl substituted pre

Antifungal and cytotoxic activities of some N-substituted aniline derivatives bearing a hetaryl fragment

Kouznetsov, Vladímir V.,Vargas Méndez, Leonor Y.,Sortino, Maximiliano,Vásquez, Yelkaira,Gupta, Mahabir P.,Freile, Mónica,Enriz, Ricardo D.,Zacchino, Susana A.

, p. 794 - 809 (2008/09/17)

Diverse N-substituted anilines bearing hetaryl fragments were easily prepared from corresponding aldimines derived from commercially available aromatic aldehydes and anilines. 2-Furyl substituted anilines showed very good antifungal activities against dermatophytes, particularly against Trichophyton rubrum (MIC = 3.12-6.25 μg/mL). In addition, all active compounds, 45-47, 73, and 74, were tested for cytotoxic activities against breast (MCF-7), lung (H-460), and central nervous system (SF-268) human cancer cell lines with the NCI-anticancer-drug screen. The activity of amines described in this paper, along with the low toxicity of most of them, shows promise for the future development of non-toxic new antimycotic agents.

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