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N-(2-methylbutyl)-2-phenylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1449232-27-2

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1449232-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1449232-27-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,2,3 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1449232-27:
(9*1)+(8*4)+(7*4)+(6*9)+(5*2)+(4*3)+(3*2)+(2*2)+(1*7)=162
162 % 10 = 2
So 1449232-27-2 is a valid CAS Registry Number.

1449232-27-2Downstream Products

1449232-27-2Relevant academic research and scientific papers

Method for preparation of amide and imide from alcohol and nitrogen Containing Compound

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Paragraph 0185; 0191, (2016/12/07)

The present invention relates to a method for preparing amide and imide from alcohol and a nitrogen containing compound and, more specifically, to a method for preparing amide and imide by using: a catalytic composition obtained by reacting a mixture of a transition metal complex and an N-heterocyclic carbene precursor with base or by reacting an N-heterocyclic carbene precursor with a mixture of a transition metal complex and base; or a transition metal complex catalyst including an N-heterocyclic carbene.

Ruthenium-catalyzed redox-neutral and single-step amide synthesis from alcohol and nitrile with complete atom economy

Kang, Byungjoon,Fu, Zhenqian,Hong, Soon Hyeok

supporting information, p. 11704 - 11707 (2013/09/02)

A completely atom-economical and redox-neutral catalytic amide synthesis from an alcohol and a nitrile is realized. The amide C-N bond is efficiently formed between the nitrogen atom of nitrile and the α-carbon of alcohol, with the help of an N-heterocyclic carbene-based ruthenium catalyst, without a single byproduct. A utility of the reaction was demonstrated by synthesizing 13C or 15N isotope-labeled amides without involvement of any separate reduction and oxidation step.

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