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Ethyl 2-(2,3,4,5,6-pentafluorophenyl)propanoate is a synthetic chemical compound with the molecular formula C11H9F5O2. It is a colorless liquid at room temperature and is characterized by its strong electron-withdrawing pentafluorophenyl group attached to a propanoate moiety. ethyl 2-(2,3,4,5,6-pentafluorophenyl)propanoate is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique reactivity and stability. Its properties, such as high lipophilicity and resistance to metabolic degradation, make it a valuable building block in the development of new molecules with potential applications in various industries.

727-53-7

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727-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 727-53-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 727-53:
(5*7)+(4*2)+(3*7)+(2*5)+(1*3)=77
77 % 10 = 7
So 727-53-7 is a valid CAS Registry Number.

727-53-7Downstream Products

727-53-7Relevant academic research and scientific papers

Metal-Free Tandem Rearrangement/Lactonization: Access to 3,3-Disubstituted Benzofuran-2-(3H)-ones

Santi, Micol,Ould, Darren M. C.,Wenz, Jan,Soltani, Yashar,Melen, Rebecca L.,Wirth, Thomas

, p. 7861 - 7865 (2019)

A novel metal-free synthesis of 3,3-disubstituted benzofuran-2-(3H)-ones through reacting α-aryl-α-diazoacetates with triarylboranes is presented. Initially, triarylboranes were successfully investigated in α-arylations of α-diazoacetates, however in the presence of a heteroatom in the ortho position, the boron enolate intermediate undergoes an intramolecular rearrangement to form a quaternary center. The intermediate cyclizes to afford valuable 3,3-disubstituted benzofuranones in good yields.

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