55480-47-2

Usage

InChI:InChI=1/C9H8BrN3O3/c1-6(14)9(10)12-11-7-2-4-8(5-3-7)13(15)16/h2-5,11H,1H3/b12-9-

Upstream product

• 50711-98-3 pentane-2,3,4-trione-3-(4-nitro-phenylhydrazone) 
• 7726-95-6 bromine 
• 127-09-3 sodium acetate 
• 64-19-7 acetic acid 
• 18804-75-6 1-(2-(4-nitrophenyl)hydrazono)propan-2-one 

Downstream Products

• 75057-28-2 1-[3-Acetyl-5-methyl-1-(4-nitro-phenyl)-1H-pyrazol-4-yl]-ethanone 
• 86380-92-9 C₁₅H₁₅N₅O₃ 
• 74519-19-0 1-(4-Nitro-phenylazo)-1-(triphenyl-λ⁵-phosphanylidene)-propan-2-one 
• 91757-48-1 N-[3-Methyl-benzo[1,4]thiazin-(2E)-ylidene]-N'-(4-nitro-phenyl)-hydrazine 
• 91757-51-6 N-[3-Methyl-benzo[1,4]oxazin-(2E)-ylidene]-N'-(4-nitro-phenyl)-hydrazine 

Relevant academic research and scientific papers

1,3-DIPOLAR CYCLOADDITION AND NUCLEOPHYLIC SUBSTITUTION REACTIONS OF C-ACETYL AND C-ETHOXYCARBONYL DERIVATIVE OF HYDRAZIDOYL BROMIDES

1,3-Dipolar cycloaddition as well as nucleophilic substitution reactions of c-acetyl and c-ethoxycarbonyl derivatives of hydrazidoyl bromides with a variety of dipolarophiles viz., alkenes, alkynes, α,β-unsaturated ketones, aldehydes azomethines and selec

Halogenation of Substituted Hydrazones. A Facile Route for the Synthesis of Some New Hydrazidoyl Halides

A wide variety of new alkyl, aryl, acyl and ethoxycarbonyl derivatives of hydrazidoyl halides have been synthesized by the electrophilic attack of the halogen atom on the corresponding hydrazone chain.The structural assignments of the products are based o