35157-75-6

Upstream product

• 60-29-7 diethyl ether 
• 861351-52-2 oxo-ethane-1,1,2-tricarboxylic acid triethyl ester 
• 100-63-0 phenylhydrazine 
• 64-17-5 ethanol 
• 104997-51-5 3-(4-bromo-phenyl)-3-cyano-2-oxo-propionic acid ethyl ester 
• 134541-15-4 Aethoxalyl-cyan-essigsaeure-aethylester 
• 95-92-1 oxalic acid diethyl ester 
• 6362-63-6 ethyl 3-cyano-3-phenylpyruvate 
• 108-86-1 bromobenzene 
• 128100-08-3 (Phenyl-ONN-azoxy)-acetic acid ethyl ester 

Downstream Products

• 20959-42-6 Ethyloxaminsaeure-phenylhydrazid 
• 40166-06-1 phenyl-oxalamic acid-(N'-phenyl-hydrazide) 
• 2844-27-1 4,4'-dimethyl-benzilic acid-(N'-phenyl-hydrazide) 
• 31180-63-9 hydroxy-di-[1]naphthyl-acetic acid-(N'-phenyl-hydrazide) 
• 831-90-3 β-N-methyloxamoylphenylhydrazine 
• 3166-50-5 2-ethyl-2-hydroxy-butyric acid-(N'-phenyl-hydrazide) 
• 3178-52-7 2-hydroxy-2-propyl-valeric acid-(N'-phenyl-hydrazide) 
• 19127-33-4 2-benzyl-2-hydroxy-3-phenyl-propionic acid-(N'-phenyl-hydrazide) 
• 3321-83-3 benzilic acid phenylhydrazide 
• 2844-26-0 2,2'-dimethoxy-benzilic acid-(N'-phenyl-hydrazide) 
• 39771-61-4 oxalic acid ethyl ester-[N'-(4-bromo-phenyl)-hydrazide] 
• 19356-03-7 2-oxo-2-(2-phenylhydrazinyl)acetamide 
• 18658-77-0 N'-phenyloxalyl bishydrazide 
• 55317-14-1 N,N-diphenylethoxalylhydrazine 

Relevant academic research and scientific papers

Synthesis, biological evaluation and molecular dynamics studies of oxadiazine derivatives as potential anti-hepatotoxic agents

Generally, herbal medicines having remarkable popularity for treating liver ailments, but they are still unacceptable because of the deprivation of herbal drug standardization. Therefore, there is a need for promising synthetic drugs to overcome the criti

Facile and convenient synthesis of aryl hydrazines via copper-catalyzed C-N cross-coupling of aryl halides and hydrazine hydrate

An efficient and convenient method for the synthesis of aryl hydrazines has been developed via copper-catalyzed cross-coupling of aryl bromides and hydrazine with a readily accessible ligand and water as a solvent. The multigram scale procedure is applicable to aryl bromides bearing both moderately electron-donating and electron-withdrawing substituents in the aromatic nucleus. No column chromatography is required to obtain aryl hydrazine hydrochlorides in good yields.

Antioxidant and DNA damage inhibition activities of 4-Aryl-N-(4-aryl-thiazol-2-yl)-5,6-dihydro-4H-1,3,4-oxadiazine-2-carboxamides

A series of 4-aryl-N-(4-pheny-thiazol-2-yl)-5,6-dihydro-4H-1,3,4-oxadiazine-2-carboxamides were synthesized by condensing 4-aryl-5,6-dihydro-4H-1,3,4-oxadiazine-2-carboxylic acid with 2-amino-4-aryl-thiazole derivatives. The newly synthesized molecules were characterized by spectral analysis and subjected to antioxidant and DNA damage inhibition studies.

N-(ALKOXYCARBONYLMETHYL)DIAZENE-N'-OXIDES AND SOME OF THEIR CONVERSIONS

Upon reaction of aliphatic and aromatic nitroso compounds with esters of N,N-dibromoglycine N-substituted N'-(alkoxycarbonylmethyl)diazene-N-oxides are formed.The ethyl ester of (2-phenyldiazene-2-oxido)acetic acid in concentrated H2SO4 is transformed int