102692-40-0

Basic information

• Product Name: 2-Propen-1-one, 1-(4-methylphenyl)-3-(4-nitrophenyl)-, (E)-
• Synonyms: (E)-1-(4-METHYLPHENYL)-3-(4-NITROPHENYL)-2-PROPEN-1-ONE;(2E)-1-(4-methylphenyl)-3-(4-nitrophenyl)prop-2-en-1-one
• CAS NO: 102692-40-0
• Molecular Formula: C₁₆H₁₃NO₃
• Molecular Weight: 267.28
• Mol File: 102692-40-0.mol
• Article Data: 19

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Propen-1-one, 1-(4-methylphenyl)-3-(4-nitrophenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 1-(4-methylphenyl)-3-(4-nitrophenyl)-, (E)-(102692-40-0)
• EPA Substance Registry System: 2-Propen-1-one, 1-(4-methylphenyl)-3-(4-nitrophenyl)-, (E)-(102692-40-0)

Safety Data

• Hazardous Substances Data: 102692-40-0(Hazardous Substances Data)

Upstream product

• 619-41-0 4-(bromoacetyl)toluene 
• 555-16-8 4-nitrobenzaldehdye 
• 122-00-9 para-methylacetophenone 
• 20691-75-2 1-p-tolyl-2-(triphenyl-λ⁵-arsanylidene)-ethanone 
• 2096-86-8 p-Tolylaceton 

Downstream Products

• 27547-04-2 (3-(4-nitrophenyl)oxiran-2-yl)(p-tolyl)methanone 
• 1772-39-0 6-nitro-2-(4-nitrophenyl)-1H-benzo[d]imidazole 
• 104-03-0 4-nitrobenzeneacetic acid 
• 99-94-5 p-Toluic acid 
• 727678-28-6 ethyl 2-acetylamino-2-cyano-3-(4-nitrophenyl)-5-oxo-5-(4-methylphenyl)pentanoate 
• 1197386-04-1 2-(p-tolylthio)-4-(4-nitrophenyl)-6-p-tolylpyridine-3-carbonitrile 
• 1296863-66-5 4,4,4-tribromo-3-(4-nitrophenyl)-1-(4-methylphenyl)butan-1-one 
• 35031-90-4 4'-methyl-4-nitro-α,β-dihydrochalcone 
• 1384736-90-6 (E)-1-(4-((1H-imidazol-1-yl)methyl)phenyl)-3-(4-nitrophenyl)prop-2-en-1-one 
• 51250-80-7 5-(4-nitro-phenyl)-3-p-tolyl-4,5-dihydro-isoxazole 
• 1394072-32-2 1-(4,5-dihydro-5-(4-nitrophenyl)-3-p-tolylpyrazol-1-yl)-2-(5-(4-methoxyphenyl)-1H-tetrazol-1-yl)ethanone 
• 30278-84-3 4'-methyl-4-aminochalcone 
• 1350728-26-5 4-(4-methylphenylurenyl)-4'-methylchalcone 
• 1350728-24-3 4-(4-fluorophenylurenyl)-4'-methylchalcone 

Relevant articles and documents

Monofunctionalized 1,3,5,7-tetraarylazaBODIPYs and their application in the synthesis of AzaBODIPY based conjugates

A series of monofunctionalized 1,3,5,7-tetraarylazaBODIPYs containing functional groups such as p-hydroxymethyl phenyl, p-hydroxyphenyl, p-cyanophenyl, p-nitrophenyl, and p-formylphenyl groups at the 1-position of the azaBODIPY core were synthesized by mi

Lewis acid catalyst system for Claisen-Schmidt reaction under solvent free condition

Ca(OTf)2 in combination with NBu4.BF4 was established to function as an efficient catalyst system for one-pot Claisen-Schmidt condensation under neat conditions. Substituted acetophenones and benzaldehydes were coupled in situ to afford their corresponding chalcones in excellent yields. The method, with a broad range of substrate tolerance and mild operational conditions can produce assorted chalcone derivatives in moderate to high yields from easily accessible starting materials.

Iron(III) phthalocyanine chloride-catalyzed oxidation-aromatization of α,β-unsaturated ketones with hydrazine hydrate: Synthesis of 3,5-disubstituted 1H-pyrazoles

We have developed an iron(III) phthalocyanine chloride-catalyzed oxidation-aromatization of α,β-unsaturated ketones with hydrazine hydrate. Various 3,5-disubstituted 1H-pyrazoles were obtained in good to excellent yields. This method offers several advantages, including room-temperature conditions, short reaction time, high yields, simple work-up procedure, and use of air as an oxidant. The catalyst can be recovered and reused five times without loss of activity.