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36244-10-7

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36244-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36244-10-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,2,4 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36244-10:
(7*3)+(6*6)+(5*2)+(4*4)+(3*4)+(2*1)+(1*0)=97
97 % 10 = 7
So 36244-10-7 is a valid CAS Registry Number.

36244-10-7Downstream Products

36244-10-7Relevant articles and documents

Palladium-catalyzed synthesis of novel trifluoromethylated quinazolinone, N-arylquinazoline and N-benzylquinazoline derivatives

Sajadi, Mahdieh Sadat,Kazemi, Elham,Darehkordi, Ali

, (2021)

A simple and palladium-catalyzed procedure for synthesis of a novel series of potentially biologically active trifluoromethyl-substituted quinazolinones and N-arylquinazoline derivatives via condensation-cyclization reaction of 2-aminobenzamide, 2-amino-N′-arylbenzimidamides and 2-amino-N′-benzylbenzimidamides with trifluoroacetimidoyl chlorides has been developed. noteworthy, this investigation showed the possible of transition-metal-catalyzed activation of trifluoroacetimidoyl chlorides as a carbon trifluoromethylated source for the synthesis of quinazolines and quinazolinone derivatives in good to excellent yields.

Method for synthesizing 2-trifluoromethyl substituted quinazolinone by multi-component one-pot method

-

Paragraph 0033-0039, (2021/03/13)

The invention discloses a method for synthesizing 2-trifluoromethyl substituted quinazolinone by a multi-component one-pot method, and the method comprises the following steps: adding a palladium catalyst, a ligand, a carbon monoxide substitute, an additi

FeCl3-Mediated Synthesis of 2-(Trifluoromethyl)quinazolin-4(3 H)-ones from Isatins and Trifluoroacetimidoyl Chlorides

Wang, Le-Cheng,Du, Shiying,Chen, Zhengkai,Wu, Xiao-Feng

, p. 5567 - 5571 (2020/07/14)

An FeCl3-mediated cascade coupling/decarbonylative annulation reaction for the efficient construction of 2-(trifluoromethyl)quinazolin-4(3H)-ones has been developed. This transformation employs readily available isatins and trifluoroacetimidoyl chlorides as the starting materials, providing a facile and practical route to diverse biologically relevant quinazolin-4(3H)-one derivatives. A plausible reaction pathway has been proposed based on the mechanistic observations.

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