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2,4(1H,3H)-Quinazolinedione, 1-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20865-83-2

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20865-83-2 Usage

Structure

Quinazolinedione core with a phenylmethyl substituent at the 1-position

Type

Chemical compound

Biological activity

Potential

Applicability

Pharmaceutical industry

Additional research needed

Yes

Check Digit Verification of cas no

The CAS Registry Mumber 20865-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,6 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20865-83:
(7*2)+(6*0)+(5*8)+(4*6)+(3*5)+(2*8)+(1*3)=112
112 % 10 = 2
So 20865-83-2 is a valid CAS Registry Number.

20865-83-2Downstream Products

20865-83-2Relevant academic research and scientific papers

Combining Isocyanides with Carbon Dioxide in Palladium-Catalyzed Heterocycle Synthesis: N3-Substituted Quinazoline-2,4(1H,3H)-diones via a Three-Component Reaction

Mampuys, Pieter,Neumann, Helfried,Sergeyev, Sergey,Orru, Romano V. A.,Jiao, Haijun,Spannenberg, Anke,Maes, Bert U. W.,Beller, Matthias

, p. 5549 - 5556 (2017/08/17)

We report a Pd-catalyzed three-component reaction of 2-bromoanilines, carbon dioxide, and isocyanides. The combination of these two readily available C1-reactants, featuring a huge difference in kinetic and thermodynamic stability, is hitherto unprecedented in transition-metal catalysis. With this one-pot three-component reaction, N3-substituted quinazoline-2,4(1H,3H)-diones are obtained in moderate to high yields in a completely regio- and chemoselective manner. Our approach easily allows variation of the arene and N3-substitution pattern of the desired heterocycle. The formal synthesis of different APIs illustrates its practical applicability. In addition, the methodology also allows for a convenient and selective 13C-labeling through the use of 13CO2. This is illustrated for [2-13C]-2,4-dichloro-6,7-dimethoxyquinazoline synthesis, a key intermediate for several APIs.

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