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Propanedioic acid, (pentafluorobenzoyl)-, diethyl ester is a complex organic compound with the chemical formula C17H15F5O4. It is a derivative of propandioic acid, where the hydrogen atoms are replaced by a pentafluorobenzoyl group and two ethyl ester groups. Propanedioic acid, (pentafluorobenzoyl)-, diethyl ester is characterized by its unique structure, which includes a central propandioic acid backbone, a pentafluorobenzoyl group that imparts significant electron-withdrawing properties, and two ethyl ester groups that contribute to its overall reactivity and solubility. It is often used in chemical research and synthesis due to its potential applications in the preparation of various pharmaceuticals and other organic compounds. The compound's properties, such as its stability and reactivity, make it a valuable intermediate in the synthesis of more complex molecules.

4404-09-5

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4404-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4404-09-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,0 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4404-09:
(6*4)+(5*4)+(4*0)+(3*4)+(2*0)+(1*9)=65
65 % 10 = 5
So 4404-09-5 is a valid CAS Registry Number.

4404-09-5Downstream Products

4404-09-5Relevant academic research and scientific papers

Structure of diethyl (polyfluorobenzoyl)malonates and their thermal intramolecular cyclization

Bazhin,Schegol'Kov,Kudyakova,Burgart,Saloutin

experimental part, p. 929 - 932 (2012/02/05)

The reaction of the C-ethoxymagnesium derivative of diethyl malonate with polyfluorobenzoyl chlorides affords the corresponding (polyfluorobenzoyl) malonates prone to thermal cyclization into coumarin derivatives. The compounds obtained are inherent in ke

7-(substituted)piperazinyl-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids

-

, (2008/06/13)

7-(substituted)piperazinyl-1-ethyl-6-fluoro-4-oxo-3-quinolinecarboxylic acids, the pharmacologically acceptable salts thereof, compositions containing them, processes and intermediates for producing them, and methods of using them to treat bacterial infections in warm-blooded animals.

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