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(1-(pyrimidin-2-yl)-1H-indol-2-yl)(4-(trifluoromethyl)phenyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1427669-89-3

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1427669-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427669-89-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,6,6 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1427669-89:
(9*1)+(8*4)+(7*2)+(6*7)+(5*6)+(4*6)+(3*9)+(2*8)+(1*9)=203
203 % 10 = 3
So 1427669-89-3 is a valid CAS Registry Number.

1427669-89-3Relevant academic research and scientific papers

Merger of Visible-Light Photoredox Catalysis and C-H Activation for the Room-Temperature C-2 Acylation of Indoles in Batch and Flow

Sharma, Upendra K.,Gemoets, Hannes P. L.,Schr?der, Felix,No?l, Timothy,Van Der Eycken, Erik V.

, p. 3818 - 3823 (2017)

A mild and versatile protocol for the C-H acylation of indoles via dual photoredox/transition-metal catalysis was established in batch and flow. The C-H bond functionalization occurred selectively at the C-2 position of N-pyrimidylindoles. This room-temperature protocol tolerated a wide range of functional groups and allowed for the synthesis of a diverse set of acylated indoles. Various aromatic as well as aliphatic aldehydes (both primary and secondary) reacted successfully. Interestingly, significant acceleration (20 to 2 h) and higher yields were obtained under micro flow conditions.

Directed Decarbonylation of Unstrained Aryl Ketones via Nickel-Catalyzed C - C Bond Cleavage

Zhao, Tian-Tian,Xu, Wen-Hua,Zheng, Zhao-Jing,Xu, Peng-Fei,Wei, Hao

, p. 586 - 589 (2018/01/26)

The nickel-catalyzed decarbonylation of unstrained diaryl ketones has been developed. The reaction is catalyzed by a combination of Ni(cod)2 and an electron-rich N-heterocyclic carbene ligand. High functional group tolerance and excellent yields (up to 98%) are observed. This strategy provides an alternative and versatile approach to construct biaryls using an inexpensive nickel catalyst.

Dual visible-light photoredox and palladium(II) catalysis for dehydrogenative C2-acylation of indoles at room temperature

Manna, Manash Kumar,Bairy, Gurupada,Jana, Ranjan

supporting information, p. 5899 - 5903 (2017/07/25)

A highly regioselective direct C2-acylation of N-pyrimidine protected indoles with aldehydes is reported at room temperature through the merger of visible light photoredox and palladium(ii) catalysis. Late-stage acylation of tryptophan, selective mono-acylation of carbazole and the syntheses of tubulin inhibitors D-64131 and D-68144 are also demonstrated.

Palladium-catalyzed decarboxylative C2-acylation of indoles with α-oxocarboxylic acids

Pan, Changduo,Jin, Hongming,Liu, Xu,Cheng, Yixiang,Zhu, Chengjian

supporting information, p. 2933 - 2935 (2013/04/24)

A palladium-catalyzed decarboxylative C2-acylation of indoles with α-oxocarboxylic acids was achieved. This protocol represents a novel and complementary approach to 2-aroylindoles. The Royal Society of Chemistry 2013.

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