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4,6-di(p-tolyl)pyrimidin-2(1H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97691-65-1

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97691-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97691-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,9 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97691-65:
(7*9)+(6*7)+(5*6)+(4*9)+(3*1)+(2*6)+(1*5)=191
191 % 10 = 1
So 97691-65-1 is a valid CAS Registry Number.

97691-65-1Downstream Products

97691-65-1Relevant academic research and scientific papers

H3PMo12O40 catalyzed three-component one-pot synthesis of 4,6-diarylpyrimidin-2(1H)-ones under solvent-free conditions

Pourghobadi, Zeinab,Derikvand, Fatemeh

experimental part, p. 269 - 272 (2010/12/19)

4,6-Diarylpyrimidin-2(1H)-one derivatives have been synthesized from three-component one-pot condensation of acetophenone derivatives, aldehydes and urea in the presence of trimethylsilyl chloride and a catalytic amount of H3PMo12Os

One-pot synthesis of 4,6-diarylpyrimidin-2(1H)-ones via multi-component reaction promoted by chlorotrimethylsilane

Wang, Lizhong,Bian, Xiaoqin,Liu, Hui,Sun, Qian,Wang, Cunde

experimental part, p. 694 - 696 (2011/04/24)

4,6-Diarylpyrimidin-2(1H)-ones were effectively synthesised by utilising chlorotrimethylsilane (TMSCI) as an efficient promoter in the cyclisation condensation of arylketones, substituted benzaldehydes and urea by a one-pot, threecomponent reaction under

Reaction of α,β-Unsaturated Ketones with Urea. Synthesis and Spectral Properties of 2(1H)-Pyrimidinone Derivatives

Sabri, Salim S.,Hussein, Ahmad Q.,Al-Hajjar, Farouk H.

, p. 512 - 514 (2007/10/02)

1,3-Diaryl-2-propen-1-ones react with urea to give 4,6-diaryl-3,4-dihydropyrimidinones (IVa-g) that can be further oxidized to the corresponding dehydro analogues (Va-f).The latter compounds are also obtained via interaction of aroylphenylacetylenes with urea.Spectral data, supporting the suggested structures IV and V, are presented.

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