100381-58-6

Basic information

• Product Name: (3,5-dimethyl-1H-pyrazol-1-yl) (o-tolyl)methanone
• Synonyms: (3,5-dimethyl-1H-pyrazol-1-yl) (o-tolyl)methanone
• CAS NO: 100381-58-6
• Molecular Weight: 214.267
• Mol File: 100381-58-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (3,5-dimethyl-1H-pyrazol-1-yl) (o-tolyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (3,5-dimethyl-1H-pyrazol-1-yl) (o-tolyl)methanone(100381-58-6)
• EPA Substance Registry System: (3,5-dimethyl-1H-pyrazol-1-yl) (o-tolyl)methanone(100381-58-6)

Safety Data

• Hazardous Substances Data: 100381-58-6(Hazardous Substances Data)

Upstream product

• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 95-49-8 2-methylchlorobenzene 
• 933-88-0 ortho-toluoyl chloride 
• 7658-80-2 2-methylbenzohydrazide 
• 123-54-6 acetylacetone 

Downstream Products

• 529-20-4 2-methylphenyl aldehyde 

Relevant articles and documents

Exploration of carboxy pyrazole derivatives: Synthesis, alkaline phosphatase, nucleotide pyrophosphatase/phosphodiesterase and nucleoside triphosphate diphosphohydrolase inhibition studies with potential anticancer profile

In the present work we report the synthesis of new aryl pyrazole derivatives using 1,3-dicarbonyl motifs. The reaction was proceeded by the cyclization of pentane-2,4-dione (1a), 3-chloropentane-2,4-dione (1b) or ethyl 3-oxobutanoate (1c) with different a

Iodonium salts as efficient iodine(iii)-based noncovalent organocatalysts for Knorr-type reactions

Hypervalent iodine(iii)-derivatives display higher catalytic activity than other aliphatic and aromatic iodine(i)- or bromine(i)-containing substrates for a Knorr-type reaction of N-acetyl hydrazides with acetyl acetone to give N-acyl pyrazoles. The highe