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Methanone, (2-methoxy-4,5-dimethylphenyl)phenyl-, also known as 1-(2-methoxy-4,5-dimethylphenyl)ethanone, is an organic compound with the chemical formula C11H14O2. It is a derivative of acetophenone, featuring a methoxy group at the 2-position and two methyl groups at the 4 and 5 positions on the phenyl ring. Methanone, (2-methoxy-4,5-dimethylphenyl)phenyl- is characterized by its aromatic structure and ketone functional group, which contributes to its reactivity and potential applications in organic synthesis. It is typically synthesized through various chemical reactions and can be used as an intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. The compound's properties, such as its boiling point, melting point, and solubility, are influenced by its molecular structure and can be important factors in its handling and use.

4072-15-5

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4072-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4072-15-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4072-15:
(6*4)+(5*0)+(4*7)+(3*2)+(2*1)+(1*5)=65
65 % 10 = 5
So 4072-15-5 is a valid CAS Registry Number.

4072-15-5Relevant academic research and scientific papers

Synthesis and evaluation of [2-(4-quinolyloxy)phenyl]methanone derivatives: Novel selective inhibitors of transforming growth factor-β kinase

Shimizu, Toshiyuki,Kimura, Kaname,Sakai, Teruyuki,Kawakami, Kazuki,Miyazaki, Tetsuko,Nakouji, Masayoshi,Ogawa, Akira,Ohuchi, Hitomi,Shimizu, Kiyoshi

supporting information; experimental part, p. 3326 - 3329 (2009/04/06)

We synthesized and evaluated various [2-(4-quinolyloxy)phenyl]methanone derivatives. These compounds had novel chemical structures that were distinct from those of previously reported inhibitors. Biological data suggested that these compounds inhibited transforming growth factor-β signaling by interacting with the ATP-binding pocket of the transforming growth factor-β type I receptor kinase domain. Here, we report on the synthesis and structure-activity relationships of the compounds in this series.

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