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5-acetyl-6-methyl-4-(2,5-dimethoxyphenyl)-3,4-dihydropyrimidin-2(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

292853-54-4

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292853-54-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 292853-54-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,2,8,5 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 292853-54:
(8*2)+(7*9)+(6*2)+(5*8)+(4*5)+(3*3)+(2*5)+(1*4)=174
174 % 10 = 4
So 292853-54-4 is a valid CAS Registry Number.

292853-54-4Relevant academic research and scientific papers

Dihydropyrimidinone/1,2,3-triazole hybrid molecules: Synthesis and anti-varicella-zoster virus (VZV) evaluation

Kaoukabi, Hanane,Kabri, Youssef,Curti, Christophe,Taourirte, Moha,Rodriguez-Ubis, Juan C.,Snoeck, Robert,Andrei, Graciela,Vanelle, Patrice,Lazrek, Hassan B.

, p. 772 - 781 (2018)

By combining the structural features of dihydropyrimidinone and 1,2,3-triazole heterocycles, novel hybrid compounds were synthesized using a simple and convenient method. A series of novel mono and bis 1,2,3-triazole was synthesized via copper-catalyzed Huisgen azide-alkyne cycloadditions (CuAAC) under microwave irradiation. The newly synthesized compounds were evaluated for their antiviral activity against varicella-zoster virus (VZV). Compounds 6aa, 7ab, 6ba and 6da showed valuable antiviral activities, with EC50 values ranging from 3.6 to 11.3 μM against TK+ and TK- VZV and without measurable cell-growth inhibition.

Regioselective chlorination at C-6 methyl position of 3,4-dihydropyrimidin- 2(1H)-ones using (dichloroiodo)benzene

Tale, Nilesh P.,Shelke, Amol V.,Bhong, Bhagyashree Y.,Karade, Nandkishor N.

, p. 981 - 986 (2013/07/26)

The reaction of (dichloroiodo)benzene with 4-aryl-1,2,3,4-tetrahydro-6- methyl-2-oxopyrimidine-5-carboxylates and 5-acetyl-4-aryl-3,4-dihydro-6- methylpyrimidin-2(1H)-ones resulted in geminal dichlorination at the C-6 methyl position of 3,4-dihydropyrimid

The development of an ecofriendly procedure for alkaline metal (II) sulfate promoted synthesis of N,N′-dimethyl substituted (unsubstituted)-4-aryl-3, 4-dihydropyrimidones (thiones) and corresponding bis-analogues in aqueous medium: evaluation by green che

Mukhopadhyay, Chhanda,Datta, Arup

experimental part, p. 136 - 146 (2010/04/23)

(Chemical Equation Presented) Different alkaline metal (II) sulfates were used as catalysts for the N,N′-dimethyl substituted as well as unsubstituted 4-aryl-3,4-dihydropyrimidones (thiones) and their corresponding bis-analogues in aqueous medium. Among t

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