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2-Hydroxy-5-bromoacetophenone isonicotinoylhydrazone is a complex organic compound with the chemical formula C14H12BrNO2. It is a derivative of acetophenone, featuring a hydroxyl group at the 2-position, a bromine atom at the 5-position, and an isonicotinoylhydrazone group attached to the carbonyl carbon. 2-hydroxy-5-bromoacetophenone isonicotinoylhydrazone is known for its potential applications in the synthesis of various pharmaceuticals and chemical research due to its unique structure and reactivity. The isonicotinoylhydrazone moiety, in particular, is significant as it can participate in various chemical reactions, such as tautomerism and metal complexation, which are important in the development of new drugs and materials. The compound's properties, such as its solubility and stability, can also be influenced by the presence of the bromine atom, making it a subject of interest in organic chemistry and medicinal chemistry research.

792-35-8

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792-35-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 792-35-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,9 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 792-35:
(5*7)+(4*9)+(3*2)+(2*3)+(1*5)=88
88 % 10 = 8
So 792-35-8 is a valid CAS Registry Number.

792-35-8Downstream Products

792-35-8Relevant academic research and scientific papers

Synthesis of hydrazones schiff bases and microbiological evaluation of lsonicotinoyl hydrazide with different acetophenone

Kelode,Mandlik,Aswar

, p. 1053 - 1062 (2012/04/04)

A series of hydrazones Schiff bases compounds have been synthesized by reacting isonicotinoyl hydrazide with 2-hydroxy-5-chloro acetophenone, 2-hydroxy-5-methyl acetophenone, 2-hydroxy-5-carboxy acetophenone, 2,5-dihydroxy acetophenone, 2-hydroxy-5-chloro-4-methyl acetophenone, 2-hydroxy-5-chloro-3- nitro acetophenone, 2-hydroxy-5-methyl-3-nitro acetophenone and 2-hydroxy-5-bromo acetophenone. The Schiff bases have been evaluated for the antifungal and antibacterial activities.

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