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1333229-86-9

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1333229-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1333229-86-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,2,2 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1333229-86:
(9*1)+(8*3)+(7*3)+(6*3)+(5*2)+(4*2)+(3*9)+(2*8)+(1*6)=139
139 % 10 = 9
So 1333229-86-9 is a valid CAS Registry Number.

1333229-86-9Downstream Products

1333229-86-9Relevant academic research and scientific papers

Novel Mannich Base Derivatives: Synthesis, Characterization, Antimicrobial and Antioxidant Activities

Kotan, Gül

, p. 830 - 841 (2022/03/01)

In this study, 3-alkyl(aryl)-4-(4-ethylbenzylidenamino)-4,5-dihydro-1H-1,2,4-triazol-5- ones 2 were synthesized as explained in the literature. Then, the Schiff bases 2 were treated with morpholine/ N-methylpiperazine/ 3-methylpiperidine/ 4-piperidinecarboxamide in the presence of formaldehyde according to the Mannich reaction to synthesize novel Mannich bases 3, 4, 5, and 6 types, respectively. The structural analyses of 24 newly synthesized compounds were characterized using proton/ carbon 13 nuclear magnetic resonance (1H/ 13C-NMR), Infrared (IR) spectoscopic techniques. In addition, the antimicrobial activity of the compounds was determined on six bacteria by using the agar well diffusion method. The most effective results against gram positive and negative bacteria were observed in 6(a-d) and 6f compounds. Also, the antioxidant capacities of the substances were investigated by three different methods (DPPH, reducing power, metal chelation). All compounds 3-6(a-f) showed a metal chelating effect.

Synthesis and in-vitro antioxidant evaluation of some novel 4-(4-substituted) benzylidenamino-4,5-dihydro-1H-1,2,4-triazol-5-ones

Yueksek, Haydar,Guersoy-Kol, Oezlem,Kemer, Guel,Ocak, Zafer,Anil, Baris

, p. 325 - 330 (2013/09/24)

3-Alkyl (aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2a-g) were reacted with 4-ethylbenzaldehyde to afford the corresponding 3-alkyl (aryl).4-(4-ethylbenzylidenamino)-4,5-dihydro-1H-1,2.4-triazol-5-ones (3a-g). The acetylation reactions of compound

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