7473-93-0

Basic information

• Product Name: 2-NITROCHALCONE
• Synonyms: 2-NITROCHALCONE;1-Phenyl-3-(2-nitrophenyl)-2-propene-1-one;3-(2-Nitrophenyl)-1-phenyl-2-propen-1-one;Phenyl(2-nitrostyryl) ketone;β-(2-Nitrophenyl)acrylophenone;3-(2-Nitrophenyl)-1-phenylprop-2-en-1-one;(2E)-3-(2-nitrophenyl)-1-phenylprop-2-en-1-one;(E)-3-(2-nitrophenyl)-1-phenyl-prop-2-en-1-one
• CAS NO: 7473-93-0
• Molecular Formula: C₁₅H₁₁NO₃
• Molecular Weight: 253.25
• Product Categories: Chalcones
• Mol File: 7473-93-0.mol
• Article Data: 48

Chemical Properties

• Melting Point: 124-128°C
• Boiling Point: 427°Cat760mmHg
• Flash Point: 205.5°C
• Appearance: /
• Density: 1.255g/cm³
• Vapor Pressure: 1.7E-07mmHg at 25°C
• Refractive Index: 1.651
• CAS DataBase Reference: 2-NITROCHALCONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-NITROCHALCONE(7473-93-0)
• EPA Substance Registry System: 2-NITROCHALCONE(7473-93-0)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 7473-93-0(Hazardous Substances Data)

Usage

Uses

(2E)-3-(2-Nitrophenyl)-1-phenylprop-2-en-1-one is a useful research chemical compound.

InChI:InChI=1/C15H11NO3/c17-15(13-7-2-1-3-8-13)11-10-12-6-4-5-9-14(12)16(18)19/h1-11H/b11-10+

Upstream product

• 54987-90-5 2-Nitrochalkondibromid 
• 552-16-9 ortho-nitrobenzoic acid 
• 93-55-0 1-phenyl-propan-1-one 
• 20913-05-7 (Benzoylmethylene)triphenylphosphorane 
• 552-89-6 2-nitro-benzaldehyde 
• 98-86-2 acetophenone 
• 634606-85-2 3-hydroxy-3-(2-nitrophenyl)-1-phenylpropane-1-one 
• 6345-63-7 1-diacetoxymethyl-2-nitro-benzene 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 536-74-3 phenylacetylene 
• 70-11-1 α-bromoacetophenone 
• 101854-90-4 [(2S,3R)-3-(2-Nitro-phenyl)-aziridin-2-yl]-phenyl-methanone 
• 611-73-4 Benzoylformic acid 
• 612-41-9 2-nitrocinnamic acid 

Downstream Products

• 612-96-4 2-Phenylquinoline 
• 54987-90-5 2-Nitrochalkondibromid 
• 79823-08-8 1,2,3,7-Tetrahydro-8-(2-imidazolin-2-yl)-7-(2-nitrophenyl)-5-phenylimidazo<1,2-a>pyridin-hydrochlorid 
• 1022-86-2 2-benzoylindole 
• 55483-95-9 (o-Nitrophenyl-1-phenyl-3-oxo-3-propylthio)-2-essigsaeureethylester 
• 5659-33-6 2-phenylquinoline 1-oxide 
• 134-81-6 benzil 
• 482-89-3 1H,1H'-2,2'-Biindolylidene-3,3'-dione 
• 108714-18-7 3-(2-aminophenyl)-1-phenyl-2-(E)-propen-1-one 
• 101854-90-4 [(2S,3R)-3-(2-Nitro-phenyl)-aziridin-2-yl]-phenyl-methanone 
• 152192-62-6 4,5-dihydro-5-(2-nitrophenyl)-3-phenyl-1H-pyrazole 
• 602308-49-6 5-(2-aminophenyl)-3-phenyl-4,5-dihydropyrazole 

Relevant articles and documents

Successive oxidation-condensation reactions using a multifunctional gold-supported nanocomposite (Au/MgCe-HDO)

The application of gold-supported nanocomposites is useful in clinical diagnostics because of their ability to provide bio-compatible and sensitive detection systems. A gold-supported magnesium hydroxide and cerium oxide nanocomposite framework (Au/MgCe-HDO) was synthesized and characterized via XRD, XPS, SEM, DLS, TEM, and TGA techniques. The nanocomposite was used as a selective catalyst for the aerobic oxidation of alcohols under mild reaction conditions followed by successive condensation reactions, like Knoevenagel and Claisen-Schmidt condensation. Substituted benzyl alcohols were converted into the corresponding carbonyl compounds in the presence of the Au/MgCe-HDO nanocomposite with O2 gas and toluene as a solvent. We observed that, upon the addition of malononitrile/ethyl cyanoacetate/acetophenone to the catalyst in the aerobic oxidation reaction, the reaction proceeds to produce the corresponding desired condensation product with up to 95% yield.

N2H4-H2O Enabled Umpolung Cyclization of o-Nitro Chalcones for the Construction of Quinoline N-Oxides

Umpolung is a unique strategy which converts the property of an atom into the opposite one. An efficient and general method for the construction of quinoline N-oxides via umpolung of carbonyl groups was developed from ortho-nitro chalcones and hydrazine i

A useful method for the conversion of olefins to nitro olefins

Triflyl nitrate is easily generated from tetra-n-butylammonium nitrate in CH2Cl2 solution and serves as an effective nitrating agent for a wide range of unsaturated substrates to form nitro olefins.