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1-benzyl-2-(naphthalen-2-yl)-1H-benzo[d]imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1310486-90-8

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1310486-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1310486-90-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,4,8 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1310486-90:
(9*1)+(8*3)+(7*1)+(6*0)+(5*4)+(4*8)+(3*6)+(2*9)+(1*0)=128
128 % 10 = 8
So 1310486-90-8 is a valid CAS Registry Number.

1310486-90-8Downstream Products

1310486-90-8Relevant academic research and scientific papers

Nickel-Catalyzed Heteroarenes Cross Coupling via Tandem C-H/C-O Activation

Wang, Ting-Hsuan,Ambre, Ram,Wang, Qing,Lee, Wei-Chih,Wang, Pen-Cheng,Liu, Yuhua,Zhao, Lili,Ong, Tiow-Gan

, p. 11368 - 11376 (2018)

Inert aryl methyl ethers as coupling components via C-O activation have been established with a Ni catalyst for C-H activation of heteroarene. The key to simultaneous C-H/C-O bond activation is the use of sterically demanding o-tolylMgBr. The protocol is effective for a wide scope of substrates including naphthyl methyl ethers, anisoles, and a variety of other heteroarene derivatives. Detailed mechanistic studies indicated that the C-O cleavage is assisted via synergistic effect of nickel and Grignard reagent in this C-H/C-O reaction, which is supported by DFT calculation. At this stage, single-electron transfer can be ruled out as a main operative process for this tandem strategy.

Copper-mediated synthesis of substituted 2-aryl-N-benzylbenzimidazoles and 2-arylbenzoxazoles via C-H functionalization/C-N/C-O bond formation

Guru, Murali Mohan,Ali, Md Ashif,Punniyamurthy, Tharmalingam

, p. 5295 - 5308 (2011/08/05)

An efficient method for the transformation of N-benzyl bisarylhydrazones and bisaryloxime ethers to functionalized 2-aryl-N-benzylbenzimidazoles and 2-arylbenzoxazoles is described. The protocol involves a copper(II)-mediated cascade C-H functionalization/C-N/C-O bond formation under neutral conditions. Substrates having either electron-donating or -withdrawing substituents undergo the cyclization to afford the target heterocycles at moderate temperature.

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