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5-(trifluoromethyl)-1-methyl-3-phenyl-1H-indazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1620816-68-3

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1620816-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1620816-68-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,8,1 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1620816-68:
(9*1)+(8*6)+(7*2)+(6*0)+(5*8)+(4*1)+(3*6)+(2*6)+(1*8)=153
153 % 10 = 3
So 1620816-68-3 is a valid CAS Registry Number.

1620816-68-3Relevant academic research and scientific papers

Palladium-Catalyzed Oxidative Arylation of 1H-Indazoles with Arenes

Gambouz, Khadija,Abbouchi, Abdelmoula El,Nassiri, Sarah,Suzenet, Franck,Bousmina, Mostapha,Akssira, Mohamed,Guillaumet, Gérald,El Kazzouli, Sa?d

supporting information, p. 7435 - 7439 (2020/11/30)

A simple method for the direct Pd(OAc)2-catalyzed oxidative arylation of inactivated 1H-indazole derivatives with simple arenes is reported. This method exhibits good reaction efficiency and good functional-group tolerance. Using the developed method, 28 arylated products were prepared in yields up to 80 %.

Palladium-catalyzed ortho-acylation of N-Nitrosoanilines with α-oxocarboxylic acids: A convenient method to synthesize N-Nitroso ketones and indazoles

Zhang, Liang,Wang, Zhe,Guo, Peiyu,Sun, Wei,Li, Ya-Min,Sun, Meng,Hua, Chengwen

supporting information, p. 2511 - 2514 (2016/05/24)

An efficient and mild protocol for regioselective synthesis of N-Nitroso aryl ketones by palladium-catalyzed direct acylation of arenes using N-Nitroso as directing groups is described. This reaction proceeded smoothly and could tolerate a variety of functional groups. Moreover, this chemistry offers a convenient access to a range of indazoles.

Palladium-catalyzed direct C7-arylation of substituted indazoles

Naas, Mohammed,El Kazzouli, Sa?d,Essassi, El Mokhtar,Bousmina, Mosto,Guillaumet, Gérald

, p. 7286 - 7293 (2014/09/16)

A novel direct C7-arylation of indazoles with iodoaryls is described using Pd(OAc)2 as catalyst, 1,10-phenanthroline as ligand, and K 2CO3 as base in refluxing DMA. Direct C7-arylation of 3-substituted 1H-indazole containing an EWG on the arene ring gave the expected products in good isolated yields. In addition, a one-pot Suzuki-Miyaura/ arylation procedure leading to C3,C7-diarylated indazoles has been developed.

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