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Ethanone, 1-[2-(2-furanyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19275-14-0

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19275-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19275-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,7 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19275-14:
(7*1)+(6*9)+(5*2)+(4*7)+(3*5)+(2*1)+(1*4)=120
120 % 10 = 0
So 19275-14-0 is a valid CAS Registry Number.

19275-14-0Downstream Products

19275-14-0Relevant academic research and scientific papers

Continuous Visible-Light Photoflow Approach for a Manganese-Catalyzed (Het)Arene C?H Arylation

Liang, Yu-Feng,Steinbock, Ralf,Yang, Long,Ackermann, Lutz

, p. 10625 - 10629 (2018)

Manganese photocatalysts enabled versatile room-temperature C?H arylation reactions by means of continuous visible-light photoflow, thus allowing for efficient C?H arylations in 30 minutes with ample scope. The robustness of the manganese-catalyzed photoflow strategy was shown by visible light-induced gram-scale synthesis, clearly outperforming the batch performance.

N-Iodosuccinimide and dioxygen in an air-enabled synthesis of 10-phenanthrenols under sunlight

Chen, Bin,Guo, Jia-Dong,Tung, Chen-Ho,Wu, Li-Zhu,Yang, Xiu-Long

supporting information, p. 7193 - 7198 (2021/09/28)

Using a catalytic amount ofN-iodosuccinimide (NIS) in combination with O2in air, an aerobic oxidative reaction was carried out to efficiently and scalably construct a series of 10-phenanthrenols under sunlight at room temperature. Mechanistic studies reveal that H2O2generatedin situwas responsible for the conversion of I2to IOH as a potential initiator for later catalytic cycle.

Interplay of ortho-with spiro-cyclisation during iminyl radical closures onto arenes and heteroarenes

McBurney, Roy T.,Walton, John C.

supporting information, p. 1083 - 1092 (2013/07/19)

Sensitised photolyses of ethoxycarbonyl oximes of aromatic and heteroaromatic ketones yielded iminyl radicals, which were characterised by EPR spectroscopy. Iminyls with suitably placed arene or heteroarene acceptors underwent cyclisations yielding phenan

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