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2-oxo-2-phenyl-N-(2,3,5-trifluorophenyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1382223-35-9

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1382223-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1382223-35-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,2,2,2 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1382223-35:
(9*1)+(8*3)+(7*8)+(6*2)+(5*2)+(4*2)+(3*3)+(2*3)+(1*5)=139
139 % 10 = 9
So 1382223-35-9 is a valid CAS Registry Number.

1382223-35-9Downstream Products

1382223-35-9Relevant academic research and scientific papers

Copper-catalyzed aerobic oxidative cross-dehydrogenative coupling of amine and α-carbonyl aldehyde: A practical and efficient approach to α-ketoamides with wide substrate scope

Zhang, Chun,Zong, Xiaolin,Zhang, Liangren,Jiao, Ning

supporting information; experimental part, p. 3280 - 3283 (2012/07/31)

A copper-catalyzed aerobic oxidative cross-dehydrogenative coupling (CDC) of amine with α-carbonyl aldehyde has been developed. Many types of amines are tolerant in this transformation leading to various α-ketoamides compounds. Wide substrate scope, CDC strategy and using air as oxidant make this transformation highly efficient and practical. Molecular oxygen acts not only as the oxidant, but also as an initiator to trigger this catalytic process. Furthermore, mechanism studies show that carbonyl group of α-carbonyl aldehyde plays a role as the directing group to facilitate this chemical process.

Copper-catalyzed aerobic oxidative coupling of aryl acetaldehydes with anilines leading to α-ketoamides

Zhang, Chun,Xu, Zejun,Zhang, Liangren,Jiao, Ning

supporting information; experimental part, p. 11088 - 11092 (2012/02/02)

Efficient and practical: The title reaction provides an efficient route to α-ketoamides compounds, which are ubiquitous structural units in a number of biologically active compounds. N-substituted anilines are suitable substrates for this transformation.

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