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N-(3-hydroxy-1-phenylprop-1-en-2-yl)acetamide is a complex organic chemical compound with the molecular formula C11H11NO2. It is characterized by a unique structure that includes a hydroxyl group, a phenyl ring, and an enamine moiety. N-(3-hydroxy-1-phenylprop-1-en-2-yl)acetamide is a derivative of acetamide, where the acetamide group is attached to a 3-hydroxy-1-phenylprop-1-en-2-yl group. The presence of the hydroxyl and enamine groups suggests potential reactivity and involvement in various chemical transformations. It may be of interest in the fields of organic synthesis, pharmaceuticals, or materials science due to its structural features and the possibility of forming hydrogen bonds or participating in conjugation. However, without specific context or application, it's challenging to provide a more detailed summary of its properties or uses.

3548-72-9

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3548-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3548-72-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3548-72:
(6*3)+(5*5)+(4*4)+(3*8)+(2*7)+(1*2)=99
99 % 10 = 9
So 3548-72-9 is a valid CAS Registry Number.

3548-72-9Relevant academic research and scientific papers

Lewis Acid-Catalyzed Nucleophilic Addition of Indoles to in Situ-Generated 2-Amidoallyl Cations

Schlegel, Marcel,Schneider, Christoph

, p. 5986 - 5992 (2017/06/07)

We report herein the first Lewis acid-catalyzed generation of 2-amidoallyl cations through ring-opening of 4-benzylidene-2-oxazolines with Sc(OTf)3. Upon nucleophilic addition of indoles, indolylenamides were obtained with yields of 60-99% and excellent (Z)-selectivity. In addition, the novel strategy was also successfully applied to pyrroles and naphthols as -nucleophiles. A Br?nsted acid-catalyzed process using TfOH formed in situ was ruled out by control experiments.

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