16619-38-8

Basic information

• Product Name: 2-Propen-1-one, 1-(2-nitrophenyl)-3-phenyl-
• Synonyms: 2-Nitro-ω-benzal-acetophenon;2-Propen-1-one, 1-(2-nitrophenyl)-3-phenyl-;2-Nitro-ω-benzyliden-acetophenon;2'-nitro-chalcone;2'-Nitro-chalkon;1-(2-nitro-phenyl)-3-phenyl-propenone;2-nitrochalcone
• CAS NO: 16619-38-8
• Molecular Formula: C15H11NO3
• Molecular Weight: 253.257
• Mol File: 16619-38-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 1-(2-nitrophenyl)-3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 1-(2-nitrophenyl)-3-phenyl-(16619-38-8)
• EPA Substance Registry System: 2-Propen-1-one, 1-(2-nitrophenyl)-3-phenyl-(16619-38-8)

Safety Data

• Hazardous Substances Data: 16619-38-8(Hazardous Substances Data)

Upstream product

• 577-59-3 2-acetylnitrobenzene 
• 100-52-7 benzaldehyde 
• 98-86-2 acetophenone 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 100-52-7 benzaldehyde 
• 65-85-0 benzoic acid 
• 482-89-3 1H,1H'-2,2'-Biindolylidene-3,3'-dione 
• 169797-22-2 1-(2-aminophenyl)-3-phenyl-propan-1-one 
• 3139-42-2 2-(phenylmethylene)benzothiophen-3(2H)-one 
• 94863-31-7 3-(2-nitrophenyl)-1,5-diphenyl--2-pyrazoline 
• 63329-72-6 (Z)-2-benzylidenebenzo[b]thiophen-3(2H)-one 

Relevant articles and documents

Synthesis, molecular modeling and biological evaluation of aza-flavanones as α-glucosidase inhibitors

An efficient acid catalyzed methodology has been employed to synthesize a variety of aza-flavanones and their α-glucosidase inhibitory activity is evaluated using acarbose, miglitol and voglibose as reference standards. Molecular modeling studies were per

Efficient construction of 3-arylquinolin-4(1H)-ones via in situ Meinwald rearrangement/intramolecular reductive cyclization of 2′-nitrochalcone epoxides

An efficient method for construction of 3-arylquinolin-4(1H)-ones via in situ Meinwald rearrangement/intramolecular reductive cyclization of 2′-nitrochalcone epoxides has been developed. The practical approach is of excellent functional groups compatibili

Synthesis and screening antimicrobial activities of novel 1,3-diaryl-3-(phenylthio)propan-1-one derivatives

In this study, a series of novel β-mercapto carbonyl derivatives (3a-j) was prepared by addition of thiophenol (2) to chalcones (1a-j) in the presence of catalytic amount of iodine (10 mol%) in CH2Cl 2. Antibacterial and antifungal in vitro properties of the synthesized compounds were tested against some human pathogenic microorganisms by employing the disk diffusion technique. For the most active compounds, also minimum inhibitory concentrations (MICs) were determined. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file.