5670-69-9

Basic information

• Product Name: (2-nitro-1-phenyl-ethenyl)benzene
• CAS NO: 5670-69-9
• Molecular Formula: C₁₄H₁₁NO₂
• Molecular Weight: 225.247
• Mol File: 5670-69-9.mol
• Article Data: 37

Chemical Properties

• Boiling Point: 335.9°Cat760mmHg
• Flash Point: 148.5°C
• Density: 1.166g/cm³
• CAS DataBase Reference: (2-nitro-1-phenyl-ethenyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (2-nitro-1-phenyl-ethenyl)benzene(5670-69-9)
• EPA Substance Registry System: (2-nitro-1-phenyl-ethenyl)benzene(5670-69-9)

Safety Data

• Hazardous Substances Data: 5670-69-9(Hazardous Substances Data)

Usage

Description

(2-nitro-1-phenyl-ethenyl)benzene, also known as beta-nitrostyrene, is a chemical compound with the molecular formula C14H11NO2. It is a yellow to orange colored solid that is sparingly soluble in water.
Used in Pharmaceutical Industry:
(2-nitro-1-phenyl-ethenyl)benzene is used as a building block for the synthesis of pharmaceuticals. It serves as a key intermediate in the production of various organic compounds that have medicinal properties.
Used in Dye and Perfume Industry:
(2-nitro-1-phenyl-ethenyl)benzene is used as an intermediate in the manufacture of dyes, perfumes, and other fine chemicals. Its unique chemical structure allows for the creation of a wide range of colors and fragrances.
Used in Chemical Research:
(2-nitro-1-phenyl-ethenyl)benzene is used as a research compound in the field of organic chemistry. It provides valuable insights into the properties and reactions of aromatic compounds.
Safety Precautions:
(2-nitro-1-phenyl-ethenyl)benzene is known to be a skin and eye irritant and should be handled with care. Additionally, it is considered to be toxic if ingested, inhaled, or absorbed through the skin. Proper safety measures, such as wearing protective clothing and using appropriate containment, should be taken when working with this compound.

Upstream product

• 530-48-3 1,1-Diphenylethylene 
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• 7475-15-2 2,2-diphenyl-2-hydroxy-1-nitroethane 
• 19244-53-2 1,1,3,3-tetraphenyl-1-butene 
• 861374-73-4 1,2-dinitro-1,1-diphenyl-ethane 
• 75-36-5 acetyl chloride 
• 509-14-8 tetranitromethane 
• 13249-58-6 1-bromo-2,2-diphenylethylene 
• 15795-74-1 1,1-diphenyl-2,2-dinitroethylene 
• 97807-43-7 1-nitro-2,2-diphenyl-1-(phenylthio)ethylene 
• 108-98-5 thiophenol 
• 599-67-7 1,1-diphenylethanol 

Downstream Products

• 3963-62-0 2,2-Diphenylethylamine 
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• 41401-03-0 diphenyl-acetaldehyde-oxime 
• 5582-87-6 β,β-diphenyl-1-nitroethane 
• 55109-45-0 2,2-Diphenyl-3-nitropropionitril 
• 125877-37-4 N-Benzylidene-2,2-diphenylvinylamine 
• 131589-76-9 diethyl (2-nitro-1,1-diphenylethyl)phosphonate 
• 116437-79-7 3-Nitro-2,2-diphenyl-propionitrile 
• 1504-16-1 3-phenyl-1H-indole 
• 947-91-1 Diphenylacetaldehyde 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 985-09-1 Bis(2,2-diphenylvinyl)amine 
• 84726-67-0 1.1-Diphenyl-2-nitro-aethyl-kation 

Relevant articles and documents

Copper-catalyzed rapid C-H nitration of 8-aminoquinolines by using sodium nitrite as the nitro source under mild conditions

A mild, rapid and efficient method for copper-catalyzed nitration of quinolines at the C5 or C7 position was reported firstly by using sodium nitrite as the nitro source. A series of nitrated quinoline derivatives were achieved in moderate to good yields

Light-Controlled Tyrosine Nitration of Proteins

Tyrosine nitration of proteins is one of the most important oxidative post-translational modifications in vivo. A major obstacle for its biochemical and physiological studies is the lack of efficient and chemoselective protein tyrosine nitration reagents. Herein, we report a generalizable strategy for light-controlled protein tyrosine nitration by employing biocompatible dinitroimidazole reagents. Upon 390 nm irradiation, dinitroimidazoles efficiently convert tyrosine residues into 3-nitrotyrosine residues in peptides and proteins with fast kinetics and high chemoselectivity under neutral aqueous buffer conditions. The incorporation of 3-nitrotyrosine residues enhances the thermostability of lasso peptide natural products and endows murine tumor necrosis factor-α with strong immunogenicity to break self-tolerance. The light-controlled time resolution of this method allows the investigation of the impact of tyrosine nitration on the self-assembly behavior of α-synuclein.

AgNO3as Nitrogen Source for Cu-Catalyzed Cyclization of Oximes with Isocyanates: A Facile Route to N-2-Aryl-1,2,3-triazoles

A versatile copper-catalyzed [3 + 1 + 1] annulation of oximes and isocyanates with AgNO3 is described. In this conversion, AgNO3 and isocyanates instead of conventional azide or diazonium reagents were used as the nitrogen source. This three-component transformation was achieved by cleaving N-O/C-H/C-N bonds and building CN/N-N bonds, which provides a strategy to prepare N-2-aryl-1,2,3-triazoles with a good substrate and functional compatibility.