30241-64-6

Upstream product

• 30241-53-3 3-methyl-1-phenylchromeno[2,3-c]pyrazol-4(1H)-one 
• 89-98-5 2-chloro-benzaldehyde 
• 89-25-8 edaravone 
• 6630-33-7 ortho-bromobenzaldehyde 
• 26260-02-6 2-iodobenzaldehyde 
• 37703-56-3 (2-chlorophenyl)(5-hydroxy-3-methyl-1-phenyl-1H-pyrazol-4-yl)methanone 
• 30241-51-1 3-methyl-5-phenoxy-1-phenyl-1H-pyrazole-4-carboxylic acid 

Relevant academic research and scientific papers

Heterocyclic analogs of xanthiones: 5,6-fused 3-methyl-1-phenylpyrano[2,3- c]pyrazol-4(1H) thiones - Synthesis and NMR (1H, 13C, 15N) data

Various [5,6]pyrano[2,3-c]pyrazol-4(1H)-thiones were synthesized in high yields by treatment of the corresponding [5,6]pyrano[2,3-c]pyrazol-4(1H)-ones with Lawesson's reagent. Detailed NMR spectroscopic studies were undertaken of the title compounds. Comp

Copper-Catalyzed Tandem O-Arylation-Oxidative Cross Coupling: Synthesis of Chromone Fused Pyrazoles

Intermolecular tandem copper-catalyzed O-arylation-oxidative acylation (cross dehydrogenative coupling-CDC) has been developed under air as an oxidant. The reaction between 2,4-dihydro-3H-pyrazol-3-ones and ortho-halo aryl carboxaldehydes furnished the co