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4,5-bis(phenylamino)cyclohexa-3,5-diene-1,2-dione is a complex organic compound with the molecular formula C18H14N2O2. It is a derivative of cyclohexa-3,5-diene-1,2-dione, also known as dihydroxymaleic anhydride, with two phenylamino groups attached at the 4 and 5 positions. 4,5-bis(phenylamino)cyclohexa-3,5-diene-1,2-dione is characterized by its conjugated diene and dione functional groups, which contribute to its chemical reactivity and potential applications in various fields, such as pharmaceuticals, dyes, and polymers. The presence of phenyl rings in the molecule also imparts specific electronic and steric properties, making it a versatile building block for the synthesis of more complex molecules.

7461-66-7

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7461-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7461-66-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7461-66:
(6*7)+(5*4)+(4*6)+(3*1)+(2*6)+(1*6)=107
107 % 10 = 7
So 7461-66-7 is a valid CAS Registry Number.

7461-66-7Relevant academic research and scientific papers

MODEL STUDIES FOR INSECT PROTEIN SCLEROTIZATION: OXIDATIVE LOSS OF THE SIDE CHAIN FROM 4-SUBSTITUTED CATECHOLS

Pyne, Stephen G.,Truscott, Roger J. W.,Maxwell, Karin,Morales, M. Carmen,Walsh, Bernadette C.,Wynn, Barbra L.

, p. 661 - 670 (2007/10/02)

The oxidation of several 4-substituted catechols in aqueous solution, pH7 in the presence of aniline results in the formation of 4,5-dianilino-1,2-benzoquinone 2 and the anil of 2 (3).The C-4 substituent is efficiently cleaved and mechanisms are proposed to account for this phenomenon based on HPLC and GC studies and the formation of N-methylaniline when these reactions were performed in the presence of sodium cyanoborohydride.The evidence suggests that the initial step involves the addition of aniline to the catechol C-4 side chain.

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