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4-[4-(dimethylamino)benzylidene]-1-phenyl-3,5-pyrazolidinedione is a complex organic compound with the molecular formula C20H20N2O2. It is a derivative of pyrazolidinedione, featuring a phenyl group at the 1-position and a dimethylamino-substituted benzylidene group at the 4-position. This chemical is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various drugs. Its structure provides a foundation for further chemical modifications, which can lead to the development of new therapeutic agents. The compound's properties, such as its reactivity and stability, are influenced by the presence of the dimethylamino group, which can participate in various chemical reactions, making it a versatile building block in organic synthesis.

4599-11-5

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4599-11-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4599-11-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,9 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4599-11:
(6*4)+(5*5)+(4*9)+(3*9)+(2*1)+(1*1)=115
115 % 10 = 5
So 4599-11-5 is a valid CAS Registry Number.

4599-11-5Downstream Products

4599-11-5Relevant academic research and scientific papers

Investigations on the Hydrolytic Stability of 4-Arylmethylidene-2-pyrazolin-5-ones

Fanghaenel, E.,Akhlaq, M. S.,Grossmann, N.

, p. 209 - 219 (2007/10/02)

The 4-Arylmethylidene-2-pyrazoline-5-ones S are not stable under aqueous alkaline conditions.By the substitution of R3 with electron donor substituents S reacts preferably yielding aldehyde A and 2-pyrazoline-5-one P, while with electron acceptor substituents S forms 4,4'-arylmethylidene-bis-2-pyrazoline-5-one B.The intermediate of hydrolysis is 4-(arylhydroxymethyl)-2-pyrazoline-5-one SOH.The second order rate constants of the reactions of S with hydroxidions and with 2-pyrazoline-5-ones P(-) are determined.The dependence of the hydrolytic decomposition of S on the pH value, substituents and temperature is suitable for the intermediate formation of SOH.

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