99358-44-8

Upstream product

• 4553-07-5 ethyl phenylcyanoacetate 

Downstream Products

• 62538-17-4 3-amino-5-hydroxy-4-phenyl-2,5-dihydro-1H-pyrazole 
• 119769-09-4 α-cyanobenzeneacetic acid 2-(aminocarbonyl) hydrazide 
• 1384439-75-1 N-(4-methoxyphenyl)-3-amino-4-phenyl-1,2-dihydropyrazolin-5-on-1-carboxamide 
• 1384439-55-7 N-cyclohexyl-3-amino-4-phenyl-1,2-dihydropyrazolin-5-on-1-carboxamide 
• 1384856-79-4 N-(1-naphthyl)-3-amino-5-oxo-4-phenyl-1H-pyrazole-1-carboxamide 
• 1384441-16-0 N-butyl-3-amino-4-phenyl-1,2-dihydropyrazolin-5-on-1-carboxamide 
• 1447274-40-9 5,7-diethyl-3-phenylpyrazolo[1,5-a]pyrimidin-2-ol 
• 1447274-41-0 5,7-diethyl-3-phenylpyrazolo[1,5-a]pyrimidin-2-yl trifluoromethane-sulfonate 
• 1447274-39-6 tert-butyl {1-[4-(5,7-diethyl-3-phenylpyrazolo[1,5-a]pyrimidin-2-yl)phenyl]cyclobutyl}carbamate 
• 1447274-35-2 1-[4-(5,7-diethyl-3-phenylpyrazolo[1,5-a]pyrimidin-2-yl)phenyl]cyclobutanamine 
• 1447274-44-3 3-phenyl-5,7-bis(trifluoromethyl)pyrazolo[1,5-a]pyrimidin-2-ol 
• 140706-31-6 5,7-dimethyl-2-hydroxy-5-phenylpyrazolo<1,5-a>pyrimidine 
• 1462982-20-2 C₁₇H₁₆N₄O₂ 
• 1462982-21-3 C₁₃H₁₄N₄O₂ 

Relevant academic research and scientific papers

Synthesis, structure, and antibacterial evaluation of new N-substituted-3-amino- 5-oxo-4-phenyl-2,5-dihydro-1 H-pyrazole-1-carbothioamides

Novel N-substituted-3-amino-5-oxo- 4-phenyl-2,5-dihydro-1 H-pyrazole-1-carbothioamide derivatives were synthesized by means of two methods. First is the cyclization reaction of 1- (cyanophenyl)acetyl-4- substituted thiosemicarbazide, and the second one is

Inhibitory effect of N-ethyl-3-amino-5-oxo-4-phenyl-2,5-dihydro-1H- pyrazole-1-carbothioamide on Haemophilus spp. planktonic or biofilm-forming cells

During this study, we have investigated in vitro activity of N-substituted-3-amino-5-oxo-4-phenyl-2,5-dihydro-1H-pyrazole-1-carbothioamide derivatives with N-ethyl, N-(4-metoxyphenyl) and N-cyclohexyl substituents against Gram-negative Haemophilus influen

Experimental and computational studies on the tautomerism of N-substituted 3-amino-5-oxo-4-phenyl-1H-pyrazolo-1-carboxamides with antibacterial activity

The tautomerism of N-substituted 3-amino-5-oxo-4-phenyl-1H-pyrazolo-1- carboxamides with antibacterial activity is studied with X-ray crystallography, IR, 1H and 13C NMR (including NOESY spectra) and quantum chemical calculations. It

Selective method for the preparation of isomeric N-alkyl and N-aryl-3(5)-amino-5(3)-hydroxy 1H-pyrazole-1-carboxamides

As part of a program to develop novel mechanism based skeletal muscle relaxants we identified 5-amino-3-hydroxy-1H-pyrazole-1-carboxyamide (1) as a potential structural lead. This highly functionalized pyrazole was prepared via a published procedure [1] (