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2-(3-chlorophenyl)-6-phenylpyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1590366-81-6

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1590366-81-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1590366-81-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,0,3,6 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1590366-81:
(9*1)+(8*5)+(7*9)+(6*0)+(5*3)+(4*6)+(3*6)+(2*8)+(1*1)=186
186 % 10 = 6
So 1590366-81-6 is a valid CAS Registry Number.

1590366-81-6Downstream Products

1590366-81-6Relevant academic research and scientific papers

Synthesis of Asymmetrical 2,6-Diarylpyridines from Linear α,β,γ,δ-Unsaturated Ketones by Addition of Ammonium Formate Followed by Annulation

Chen, Rener,Gao, Yejun,Ma, Yongmin

, p. 3875 - 3882 (2019/10/11)

A simple and efficient method has been established for the synthesis of asymmetrical 2,6-diarylpyridines by cyclization of α,β,γ,δ-unsaturated ketones with ammonium formate under air atmosphere. The reaction is metal-free and operationally convenient from readily available starting materials. Thirty-three examples have been presented, most of which show good yields.

Copper-catalyzed direct C-H arylation of pyridine N-oxides with arylboronic esters: One-pot synthesis of 2-arylpyridines

Shen, Yan,Chen, Jiuxi,Liu, Miaochang,Ding, Jinchang,Gao, Wenxia,Huang, Xiaobo,Wu, Huayue

supporting information, p. 4292 - 4295 (2014/04/17)

The first example of the copper-catalyzed direct C-H arylation of pyridine N-oxides with arylboronic esters has been developed, leading to a wide range of 2-arylpyridines in a one-pot synthesis with moderate to good yields without an additional reductant. This transformation allows for rapid access to a variety of 2-arylpyridines using an inexpensive catalytic system that would be more difficult to access with traditional methods. Thus, this method represents a simple and practical procedure to access 2-arylpyridines.

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