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Phenyl (2-phenoxy)benzoate, also known as 2-phenoxybenzoic acid phenyl ester, is an organic compound with the chemical formula C19H16O3. It is a white crystalline solid that is soluble in organic solvents and has a molecular weight of 292.32 g/mol. phenyl (2-phenoxy)benzoate is characterized by a benzoate group attached to a phenyl ring, with a second phenyl ring connected to the benzoate through an oxygen atom. Phenyl (2-phenoxy)benzoate is used in various applications, including as a chemical intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed in the production of certain dyes and pigments. Due to its aromatic structure and ester functionality, it exhibits properties such as UV absorption, which can be leveraged in the development of light-sensitive materials.

7120-45-8

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7120-45-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7120-45-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,2 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7120-45:
(6*7)+(5*1)+(4*2)+(3*0)+(2*4)+(1*5)=68
68 % 10 = 8
So 7120-45-8 is a valid CAS Registry Number.

7120-45-8Relevant academic research and scientific papers

Decarbonylative Methylation of Aromatic Esters by a Nickel Catalyst

Okita, Toshimasa,Muto, Kei,Yamaguchi, Junichiro

supporting information, p. 3132 - 3135 (2018/05/28)

A Ni-catalyzed decarbonylative methylation of aromatic esters was achieved using methylaluminums as methylating agents. Dimethylaluminum chlorides uniquely worked as the methyl source. Because of the Lewis acidity of aluminum reagents, less reactive alkyl esters could also undergo the present methylation. By controlling the Lewis acidity of aluminum reagents, a chemoselective decarbonylative cross-coupling between alkyl esters and phenyl esters was successful.

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