94692-06-5

Basic information

• Product Name: 1H-Pyrazole-4-carboxylic acid, 1-phenyl-5-(1H-pyrrol-1-yl)-, hydrazide
• Synonyms: HMS2716N19;1H-Pyrazole-4-carboxylic acid,1-phenyl-5-(1H-pyrrol-1-yl)-,hydrazide;1-phenyl-5-(pyrrol-1-yl)-1H-pyrazole-4-carbohydrazide;1-phenyl-5-(1H-pyrrol-1-yl)-1H-pyrazole-4-carbohydrazide
• CAS NO: 94692-06-5
• Molecular Formula: C14H13N5O
• Molecular Weight: 267.28600
• Mol File: 94692-06-5.mol
• Article Data: 2

Chemical Properties

• Density: 1.35±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 1H-Pyrazole-4-carboxylic acid, 1-phenyl-5-(1H-pyrrol-1-yl)-, hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrazole-4-carboxylic acid, 1-phenyl-5-(1H-pyrrol-1-yl)-, hydrazide(94692-06-5)
• EPA Substance Registry System: 1H-Pyrazole-4-carboxylic acid, 1-phenyl-5-(1H-pyrrol-1-yl)-, hydrazide(94692-06-5)

Safety Data

• Hazardous Substances Data: 94692-06-5(Hazardous Substances Data)

Upstream product

• 100-63-0 phenylhydrazine 
• 94692-05-4 ethyl 1-phenyl-5-(pyrrol-1-yl)-1H-pyrazole-4-carboxylate 
• 16078-71-0 ethyl 5-amino-1-phenyl-1H-pyrazole-4-carboxylate 

Downstream Products

• 94692-13-4 N,N'-bis<1-phenyl-5-(pyrrol-1-yl)pyrazol-4-yl>urea 
• 94691-80-2 (1-Phenyl-1H-pyrazolo[4,3-e]pyrrolo[1,2-a]pyrazin-5-yl)-hydrazine 
• 94692-14-5 5-oxo-1-phenylpyrazolo<4,3-e>pyrrolo<1,2-a>pyrazine 
• 94692-15-6 5-Chloro-1-phenyl-1H-pyrazolo[4,3-e]pyrrolo[1,2-a]pyrazine 
• 94692-08-7 ethyl N-[1-phenyl-5-(pyrrol-1-yl)-1H-pyrazol-4-yl]carbamate 
• 94692-10-1 N-[1-phenyl-5-(pyrrol-1-yl)-1H-pyrazol-4-yl]formamide 
• 94692-09-8 1-phenyl-5-(1H-pyrrol-1-yl)-1H-pyrazol-4-ylamine 
• 867289-00-7 1-[1-phenyl-5-(pyrrol-1-yl)-1H-pyrazol-4-yl]-3-(p-tolyl)urea 

Relevant articles and documents

Synthesis, reactions and antimicrobial activity of some new 1,3,4-oxadiazoles, 1,2,4-triazoles and 1,3,4-thiadiazines derived from pyrazole

New 1,3,4-oxadiazoles, 1,2,4-triazoles and 1,3,4-thiadiazines containing a pyrazolyl moiety 7-14 were prepared using ethyl 5-amino-1-phenyl-1H-pyrazole-3- carboxylate 1 as a starting material. The newly synthesized compounds were screened for their in vitro anti-bacterial and anti-fungal activity.