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1-oxo-2-(4-nitrophenyl)-4-(4-tolyl)-1,2-dihydrophthalazine is a complex organic compound with the molecular formula C21H16N2O3. It is a derivative of phthalazine, a heterocyclic aromatic compound consisting of a diazine fused to a benzene ring. The structure of 1-oxo-2-(4-nitrophenyl)-4-(4-tolyl)-1,2-dihydrophthalazine features a 4-nitrophenyl group attached to the 2-position and a 4-tolyl group attached to the 4-position of the phthalazine core. The 1-oxo group indicates the presence of a carbonyl group at the 1-position, and the compound is in a 1,2-dihydro form, which means it has two hydrogen atoms added to the aromatic ring, reducing its conjugation. 1-oxo-2-(4-nitrophenyl)-4-(4-tolyl)-1,2-dihydrophthalazine may have potential applications in the fields of pharmaceuticals, dyes, or materials science due to its unique structure and properties.

57709-79-2

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57709-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57709-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,0 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57709-79:
(7*5)+(6*7)+(5*7)+(4*0)+(3*9)+(2*7)+(1*9)=162
162 % 10 = 2
So 57709-79-2 is a valid CAS Registry Number.

57709-79-2Downstream Products

57709-79-2Relevant academic research and scientific papers

REACTION OF 2-AROYLBENZOIC ACIDS WITH 4-NITRO- AND 2,4-DINITROPHENYLHYDRAZINE

Yakovlev, S. V.,Pavlova, L. A.

, p. 2195 - 2197 (2007/10/02)

The action of 2,4-dinitrophenylhydrazine on aroylbenzoic acids leads to the formation of stable 2,4-dinitrophenylhydrazones, which are dehydrated when heated with acetic anhydride and sodium acetate and converted into 1-oxo-2-(2,4-dinitrophenyl)-4-aryl-1,2-dihydrophthalazines.The hydrazones were not obtained in the reaction with 4-nitrophenylhydrazine.The products had 1-oxo-1,2-dihydrophthalazine structures.

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