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imidazo[1.2-a]pyridin-3-yl(p-tolyl)methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1284293-38-4

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1284293-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1284293-38-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,4,2,9 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1284293-38:
(9*1)+(8*2)+(7*8)+(6*4)+(5*2)+(4*9)+(3*3)+(2*3)+(1*8)=174
174 % 10 = 4
So 1284293-38-4 is a valid CAS Registry Number.

1284293-38-4Downstream Products

1284293-38-4Relevant academic research and scientific papers

I2-Catalyzed Three-Component Consecutive Reaction for the Synthesis of 3-Aroylimidazo[1,2-a]-N-Heterocycles

Zhang, Yi,Chen, Rener,Wang, Zhiming,Wang, Lei,Ma, Yongmin

, p. 6239 - 6246 (2021/05/07)

A convenient one-pot, three-component reaction has been developed for the synthesis of 3-aroylimidazo[1,2-a]-N-heterocycles from aryl ketones and 2-amino-N-heterocycles using dimethyl sulfoxide as a methylene donor. The reaction proceeds smoothly catalyze

I2-catalyzed intramolecular oxidative amination of C(sp3)-H bond: Efficient access to 3-acylimidazo[1,2-: A] pyridines under neat condition

Huang, Lilan,Yin, Wenqing,Wang, Jian,Gan, Chunfang,Huang, Yanmin,Huang, Chusheng,He, Yimiao

, p. 2381 - 2385 (2019/02/01)

An efficient and "green" protocol for the synthesis of 3-acylimidazo[1,2-a]pyridines through intramolecular oxidative α-amination of carbonyl compounds has been developed. The reaction proceeds smoothly utilizing I2 as a catalyst and H2O2 as an oxidant under neat condition with broad substrate scope. Several complex nitrogen-containing fused rings are conveniently constructed, which are not easy to access by traditional methods.

Iron(III)-catalyzed synthesis of 3-aroylimidazo[1,2-a]pyridines from 2-aminopyridines and ynals

Chen, Zhengwang,Liu, Botao,Liang, Pei,Yang, Zhixiong,Ye, Min

supporting information, p. 667 - 670 (2018/01/17)

An efficient iron-catalyzed intermolecular aminooxygenation of 2-aminopyridines with a wide range of ynals has been developed. 3-Aroylimidazo[1,2-a]pyridines containing various functional groups are synthesized under the standard conditions. The transformation is conducted in simple conditions and forms products in good yields.

Copper-catalyzed intramolecular oxidative amination of enaminone C-H bond for the synthesis of imidazo[1,2-a]pyridines

Wan, Jie-Ping,Hu, Deqing,Liu, Ying,Li, Luyao,Wen, Chengping

supporting information, p. 2880 - 2883 (2016/06/14)

The intramolecular C-N bond forming cross coupling reactions on the enaminones has been achieved for the synthesis of imidazole[1,2-a]pyridines via copper-catalyzed C(sp2)-H amination. This protocol provides a new route for the synthesis of 2-u

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