13808-75-8

Basic information

• Product Name: 1-(2,4-dinitrophenyl)-4-methylpyrazole
• Synonyms: 1-(2,4-dinitrophenyl)-4-methylpyrazole
• CAS NO: 13808-75-8
• Molecular Weight: 248.198
• Mol File: 13808-75-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(2,4-dinitrophenyl)-4-methylpyrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4-dinitrophenyl)-4-methylpyrazole(13808-75-8)
• EPA Substance Registry System: 1-(2,4-dinitrophenyl)-4-methylpyrazole(13808-75-8)

Safety Data

• Hazardous Substances Data: 13808-75-8(Hazardous Substances Data)

Upstream product

• 10602-37-6 1,1,3,3-tetraethoxy-2-methyl-propane 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 

Downstream Products

• 51-28-5 2,4-Dinitrophenol 
• 961-68-2 N-phenyl-2,4-dinitroaniline 
• 20916-37-4 2-(2,4-dinitrophenoxy)-N-phenylacetamide 
• 1246929-30-5 1-(2,4-dinitrophenyl)-4-methyl-5-nitropyrazole 
• 346457-44-1 2-[(2,4-dinitrophenyl)thio]-N-phenylacetamide 
• 1246929-35-0 (E)-2-[1-(2,4-dinitrophenyl)-3,5-dinitropyrazol-4-yl]-N,N-dimethylethen-1-amine 
• 1246929-36-1 (Z)-(hydroxyimino)[1-(2,4-dinitrophenyl)-3,5-dinitropyrazol-4-yl]acetaldehyde 
• 1246929-39-4 1-(2,4-dinitrophenyl)-4-[(E)-2-(4-methoxyphenyl)vinyl]-3,5-dinitropyrazole 
• 1246929-41-8 4-[(E)-2-(3,4-dimethoxyphenyl)vinyl]-1-(2,4-dinitrophenyl)-3,5-dinitropyrazole 
• 1246929-43-0 1-(2,4-dinitrophenyl)-4-[(E)-2-(4-fluorophenyl)vinyl]-3,5-dinitropyrazole 
• 4096-88-2 1-azido-2,4-dinitrobenzene 
• 58333-00-9 1-(2,4-dinitrophenyl)-4-methyl-3,5-dinitropyrazole 

Relevant articles and documents

Nitropyrazoles 15.* Synthesis and some transformations of 1-(2,4-dinitrophenyl)-4-methyl-3,5-dinitropyrazole

The method for preparation of 1-(2,4-dinitrophenyl)-4-methyl-3,5- dinitropyrazole has been developed. Due to the larger CH-acidity of 4-Me-group compared to 1,4-dimethyl-3,5-dinitropyrazole, 1-(2,4-dinitrophenyl)-4-methyl-3, 5-dinitropyrazole is capable of reacting with substituted benzaldehydes to afford 4-[(E)-2-arylvinyl]-1-(2,4-dinitrophenyl)-3,5-dinitropyrazoles. Under the action of nucleophiles, dinitrophenyl group is detached from the former compounds leading to previously unknown N-unsubstituted 4-[(E)-2-arylvinyl]-3,5- dinitropyrazoles.