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4,5-Dihydroxy-4,5-diphenylimidazolidin-2-on, also known as 4,5-Dihydroxy-4,5-diphenylimidazolidin-2-one, is a chemical compound with the molecular formula C15H14N2O4. It is a white crystalline solid that is soluble in water and various organic solvents. 4,5-Dihydroxy-4,5-diphenylimidazolidin-2-on is characterized by its imidazolidinone ring structure, which features two hydroxyl groups at the 4 and 5 positions, and two phenyl groups attached to the same positions. It is often used in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity. The compound's properties, such as its stability and potential applications, make it a subject of interest in chemical research and development.

5157-13-1

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5157-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5157-13-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,5 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5157-13:
(6*5)+(5*1)+(4*5)+(3*7)+(2*1)+(1*3)=81
81 % 10 = 1
So 5157-13-1 is a valid CAS Registry Number.

5157-13-1Relevant academic research and scientific papers

A convenient preparation of symmetrical and unsymmetrical 1,2-diketones: Application to fluorinated phenytoin synthesis

Page,Graham,Park

, p. 7265 - 7274 (2007/10/02)

1,2-Diketones are efficiently produced in two steps by reaction of aldehydes with anions derived from 2-substituted dithianes followed by treatment of the resulting alcoholis with NBS in aqueous acetone; phenytoin derivatives were prepared from these diketones by a standard method involving treatment with urea and potassium hydroxide under reflux.

Concerning the reaction mechanism of the hydantoin synthesis according to Biltz, I: Proof of the intermediates

Schwenker,Guo,Bernhart

, p. 779 - 783 (2007/10/02)

The reaction mechanism of the rearrangement occurring during the hydantoin synthesis according to Biltz, proposed by Butler and Leitch, has been ascertained. The intermediate 3a, already proposed by Biltz, could be isolated out of the reaction mixture. Th

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