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4-bromo-benzaldehyde-(4-nitro-phenylhydrazone) is a complex organic compound with the molecular formula C13H10BrN3O2. It is formed by the reaction of 4-bromobenzaldehyde with 4-nitrophenylhydrazine, resulting in the formation of a hydrazone derivative. 4-bromo-benzaldehyde-(4-nitro-phenylhydrazone) is characterized by its yellow crystalline appearance and is soluble in common organic solvents such as ethanol and acetone. It is often used in the synthesis of various pharmaceuticals and chemical intermediates due to its unique chemical properties and reactivity. The presence of both bromine and nitro groups in the molecule makes it a valuable building block for the development of new compounds with potential applications in various fields, including medicine and materials science.

5802-78-8

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5802-78-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5802-78-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,0 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5802-78:
(6*5)+(5*8)+(4*0)+(3*2)+(2*7)+(1*8)=98
98 % 10 = 8
So 5802-78-8 is a valid CAS Registry Number.

5802-78-8Relevant academic research and scientific papers

Synthesis of substituted 1 H-indazoles from arynes and hydrazones

Li, Pan,Wu, Chunrui,Zhao, Jingjing,Rogness, Donald C.,Shi, Feng

experimental part, p. 3149 - 3158 (2012/07/14)

The 1H-indazole skeleton can be constructed by a [3 + 2] annulation approach from arynes and hydrazones. Under different reaction conditions, both N-tosylhydrazones and N-aryl/alkylhydrazones can be used to afford a variety of indazoles. The former reaction affords 3-substituted indazoles either via in situ generated diazo compounds or through an annulation/elimination process. The latter reaction leads to 1,3-disubstituted indazoles likely through an annulation/oxidation process. The reactions operate under mild conditions and can accommodate aryl, vinyl, and less satisfactorily, alkyl groups.

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