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Ethyl 5-oxo-2,3-diphenylcyclopentanecarboxylate is a complex organic compound with the chemical formula C19H18O3. It is a derivative of cyclopentane, featuring a five-membered carbon ring with two phenyl groups attached at positions 2 and 3, and a carboxylate group at position 5. The molecule also contains an ethyl ester group, which is attached to the carboxylate. ethyl 5-oxo-2,3-diphenylcyclopentanecarboxylate is characterized by its unique structure and properties, making it a potential candidate for various chemical and pharmaceutical applications. Its synthesis and reactivity are of interest to researchers in the field of organic chemistry, as it can be used as a building block for more complex molecules or as a precursor in the synthesis of pharmaceuticals.

7356-94-7

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7356-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7356-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7356-94:
(6*7)+(5*3)+(4*5)+(3*6)+(2*9)+(1*4)=117
117 % 10 = 7
So 7356-94-7 is a valid CAS Registry Number.

7356-94-7Relevant academic research and scientific papers

Mechanistic Studies of Diastereoselective Cyclopropanation via Homochiral Ketals. 1. Dioxolane Structural Effects

Mash, Eugene A.,Hemperly, Susan B.,Nelson, Keith A.,Heidt, Philip C.,Deusen, Shawne Van

, p. 2045 - 2055 (2007/10/02)

Compounds structurally related to 2-cyclohexen-1-one 1,4-di-O-benzyl-L-threitol ketal were prepared and subjected to the Simmons-Smith cyclopropanation.From these experiments a mechanistic model for diastereoselective cyclopropanation of common ring syste

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