1333899-72-1

Basic information

• Product Name: 3-methyl-5-phenoxy-1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde
• Synonyms: 3-methyl-5-phenoxy-1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde
• CAS NO: 1333899-72-1
• Molecular Weight: 292.337
• Mol File: 1333899-72-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-methyl-5-phenoxy-1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methyl-5-phenoxy-1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde(1333899-72-1)
• EPA Substance Registry System: 3-methyl-5-phenoxy-1-(4-methylphenyl)-1H-pyrazole-4-carbaldehyde(1333899-72-1)

Safety Data

• Hazardous Substances Data: 1333899-72-1(Hazardous Substances Data)

Upstream product

• 86-92-0 3-methyl-1-(4-methylphenyl)-2-pyrazolin-5-one 
• 350997-70-5 5-chloro-3-methyl-1-(p-tolyl)-1H-pyrazole-4-carbaldehyde 
• 108-95-2 phenol 

Downstream Products

• 1333899-92-5 2-amino-4-(3-methyl-5-phenoxy-1-(4-methylphenyl)-1H-pyrazol-4-yl)-5-oxo-4,5-dihydropyrano[3,2-c]chromene-3-carbonitrile 
• 1333900-09-6 2-amino-4-(3-methyl-5-phenoxy-1-(4-methylphenyl)-1H-pyrazol-4-yl)-9-methyl-5-oxo-4,5-dihydropyrano[3,2-c]chromene-3-carbonitrile 
• 1427518-84-0 1-amino-3-[3-methyl-1-(4-methylphenyl)-5-phenoxy-1H-pyrazol-4-yl]-7-methylpyrido[1,2-a]benzimidazole-2,4-dicarbonitrile 
• 1427518-76-0 1-amino-3-[3-methyl-1-(4-methylphenyl)-5-phenoxy-1H-pyrazol-4-yl]pyrido[1,2-a]benzimidazole-2,4-dicarbonitrile 
• 1417913-92-8 C₂₉H₂₈N₄O₃ 
• 1417913-84-8 C₂₇H₂₄N₄O₃ 

Relevant articles and documents

Design, synthesis, and antibacterial evaluation of new Schiff's base derivatives bearing nitroimidazole and pyrazole nuclei as potent E. coli FabH inhibitors

New Schiff's base derivatives 5a-j have been synthesized by reaction between 5-aryloxypyrazole-4-carbaldehydes 3a-j and 2-(2-methyl-5-nitro-1Himidazol- 1-yl)acetohydrazide 4 in the presence of nickel (II) nitrate as a catalyst in ethanol at room temperatu

Microwave-assisted synthesis of novel 4H-chromene derivatives bearing phenoxypyrazole and their antimicrobial activity assessment

A new series of 4H-chromene derivatives 4a-p bearing the 5-phenoxypyrazole nucleus were synthesized under microwave irradiation by the reaction of 5-phenoxypyrazole-4-carbaldehydes 1a-h, malononitrile 2 and compounds 1,3-cyclohexanedione and dimedone (3a