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(E)-N-hydroxy-N-phenylcinnamamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128917-47-5

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128917-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128917-47-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,9,1 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 128917-47:
(8*1)+(7*2)+(6*8)+(5*9)+(4*1)+(3*7)+(2*4)+(1*7)=155
155 % 10 = 5
So 128917-47-5 is a valid CAS Registry Number.

128917-47-5Downstream Products

128917-47-5Relevant academic research and scientific papers

N-heterocyclic carbene (NHC)-catalyzed direct amidation of aldehydes with nitroso compounds

Fong, Tian Wong,Patra, Pranab K.,Seayad, Jayasree,Zhang, Yugen,Ying, Jackie Y.

supporting information; experimental part, p. 2333 - 2336 (2009/05/26)

(Chemical Equation Presented) NHC-catalyzed direct amidation of aldehydes with nitroso compounds is a powerful method for the synthesis of N-arylhydroxamic acids. A variety of aryl, alkyl, alkenyl, and heterocyclic aldehydes were found to give excellent yields of the corresponding N-arylhydroxamic acids. This chemistry was also extended to the synthesis of chiral N-arylhydroxamic acids by kinetic resolution of α-branched aldehydes, a domino amidation-redox amination reaction of acrolein, and a three-component reaction for the synthesis of N-arylaziridines.

N-HETEROCYCLIC CARBENE (NHC) CATALYZED SYNTHESIS OF HYDROXAMIC ACIDS

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Page/Page column 34, (2008/12/07)

A process for preparing hydroxamic acids is provided. The process comprises reacting an aldehyde with a nitroso compound in the presence of a N-heterocyclic carbene (NHC) catalyst.

A Novel Conversion of N-Aryl-N-methoxyamides into N-Arylhydroxamic Acids Using AlCl3/Thiol System

Kawase, Masami,Kitamura, Takahiro,Shimada, Masahiro,Kikugawa, Yasuo

, p. 887 - 892 (2007/10/02)

Treatment of N-aryl-N-methoxyamides with AlCl3 in EtSH (or Me2S) generates the corresponding N-aryl-N-hydroxyamides in high yields.

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