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3H-1,2,4-Triazol-3-one, 4-amino-2,4-dihydro-5-[(4-methylphenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

147440-64-0

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147440-64-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147440-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,4,4 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 147440-64:
(8*1)+(7*4)+(6*7)+(5*4)+(4*4)+(3*0)+(2*6)+(1*4)=130
130 % 10 = 0
So 147440-64-0 is a valid CAS Registry Number.

147440-64-0Upstream product

147440-64-0Relevant academic research and scientific papers

Synthesis of novel triazol compounds containing isatin as potential antibacterial and antifungal agents by microwave and conventional methods

Oezil, Musa,Mentese, Emre,Yilmaz, Fatih,Islamoglu, Fatih,Kahveci, Bahittin

, p. 268 - 271 (2011)

Microwave irradiation has been used to accelerate the conversion of isatin (1a) and 5-nitroisatin (1b) into their Schiff bases 3-[5′-aryl(alkyl)- 2′,4′-dihydro-1′,2′,4′-triazol-3′-on- 4′-yl]iminoisatin (3a-g) and 3-[5′-aryl(alkyl)-2′,4′- dihydro-1′,2′,4′-triazol-3′-on-4′-yl] imino-5-nitroisatin (4a-g), respectively. Reaction was achieved by microwave-induced technique, which reduced the reaction time drastically and improved the yield when compared to conventional heating. The newly synthesised bases showed moderate antimicrobial activity against the standard bacterial and fungal organisms tested.

Synthesis, in vitro antimicrobial and antioxidant activities of some new 4,5-dihydro-1h-1,2,4-triazol-5-one derivatives

Yueksek, Haydar,Akyildirim, Onur,Yola, Mehmet L.,Guersoy-Kol, Oezlem,Celebier, Mustafa,Kart, Didem

, p. 470 - 480 (2013)

A series of compounds derived from 4,5-dihydro-1H-1,2,4-triazol-5-one were synthesized and characterized by spectral data. The 12 new compounds were analyzed for their potential in vitro antioxidant activities by three different methods. Compound 4f showe

Synthesis and in vitro antioxidant and antimicrobial activities of novel 3-alkyl(aryl)-4-[3-methoxy-4-(2-furylcarbonyloxy)-benzylidenamino]-4,5-dihydro-1H-1,2,4-triazol-5-ones, and their N-acetyl, N-Mannich base derivatives

Manap, Sevda

, (2021/09/03)

The reactions of 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (1) with 3-methoxy-4-(2-furylcarbonyloxy)-benzaldehyde (2) formed 3-alkyl(aryl)-4-[3-methoxy-4-(2-furylcarbonyloxy)-benzylidenamino]-4,5-dihydro-1H-1,2,4-triazol-5-ones (3). Moreov

In vitro antioxidant and antimicrobial properties of some new 4,5-dihydro-1H-1,2,4-triazole-5-ones

Akta?-Yoku?,Yüksek,Gürsoy-Kol,Alpay-Karao?lu

, p. 389 - 396 (2018/09/29)

In this study, 3-alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (3a-3h) reacted with 3-benzenesulfonyloxy-4-methoxybenzaldehyde (1a-1h) to afford eight new 3-alkyl(aryl)-4-(3-benzenesulfonyloxy-4-methoxybenzylidenamino)-4,5-dihydro-1H-1,2,4-triaz

Study of antioxidant properties and DNA interaction of some novel 4,5-Dihydro-1H-1,2,4-triazol-5-one derivatives

Arslantas, Ali,Yüksek, Haydar,Gürsoy-Kol, ?zlem,Ocak, Zafer,Tomruk, Zeynep,Calapoglu, Mustafa

scheme or table, p. 3327 - 3334 (2012/07/28)

3-Alkyl(aryl)-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (2) reacted with 4-benzenesulfonyloxybenzaldehyde (3) to afford the corresponding seven novel 3-alkyl(aryl)-4-(4-benzenesulfonyloxybenzylidenamino)-4,5-dihydro-1H-1,2, 4-triazol-5-ones (4). The ace

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

Synthesis and in vitro antioxidant evaluation of some novel 4, 5-dihydro-1h-1, 2, 4-triazol-5-one derivatives

Gursoy Kol,Yuksek

experimental part, p. 123 - 136 (2011/01/03)

In this study, thirteen novel 4,5-dihydro-1H-1,2,4-triazol-5-one derivatives were synthesized and characterized by elemental analyses and IR, 1H NMR,13C NMR and UV spectral data. The synthesized compounds were analyzed for their in v

Determination of the protonation constants of some 4-(substituted benzylamino)-4,5-dihydro-1H-1,2,4-triazol-5-ones by the potentiometric method in ethanol-water mixtures

Islamoglu, Fatih,Kahveci, Bahittin,Islamoglu, Yahya

, p. 36 - 41 (2008/09/17)

To gain more information about the effect of solvent on 4,5-dihydro-1H-1,2,4-triazol-5-ones, the stoichiometric protonation constants of thirteen triazoles in ethanol-water mixtures were determined at an ionic strength of 0.10MNaCl and at 25.0 ± 0.1°C und

Synthesis and antitumor activities of some 4,5-dihydro-1H-1,2,4-triazol-5-ones

Ikizler, Aykut A.,Ikizler, Aysun,Serdar, Mevluet,Yildirim, Nuri

, p. 363 - 370 (2007/10/03)

Eight new 3-alkyl(aryl)-4-arylidenamino-4,5-dihydro-1H-1,2,4-triazol-5-ones were synthesized and characterised by elemental analysis, 1H NMR, IR and UV spectra. Seven new and 34 recently reported derivatives of 4,5-dihydro-1H-1,2,4-triazol-5-one ring were screened for their antitumor activities.

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