134538-46-8

Basic information

• Product Name: Benzene, 1-fluoro-4-[(1E)-2-nitro-1-propenyl]-
• Synonyms: 1-(4-fluorophenyl)-2-nitropropene;2-Nitro-1-(4-fluor-phenyl)-propen-(1);1-(4-Fluor-phenyl)-2-nitro-prop-1-en;1-fluoro-4-(2-nitro-1-propenyl)benzene;1-(p-fluorophenyl)-2-nitropropene;Benzene,1-fluoro-4-(2-nitro-1-propen-1-yl)
• CAS NO: 134538-46-8
• Molecular Formula: C9H8FNO2
• Molecular Weight: 181.166
• Mol File: 134538-46-8.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Benzene, 1-fluoro-4-[(1E)-2-nitro-1-propenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-fluoro-4-[(1E)-2-nitro-1-propenyl]-(134538-46-8)
• EPA Substance Registry System: Benzene, 1-fluoro-4-[(1E)-2-nitro-1-propenyl]-(134538-46-8)

Safety Data

• Hazardous Substances Data: 134538-46-8(Hazardous Substances Data)

Upstream product

• 79-24-3 Nitroethane 
• 459-57-4 4-fluorobenzaldehyde 
• 135711-46-5 Butyl-[1-(4-fluoro-phenyl)-2-nitro-propyl]-amine 
• 140-75-0 para-fluorobenzylamine 
• 459-56-3 4-fluorobenzylic alcohol 
• 593-51-1 methylamine hydrochloride 
• 222025-82-3 1-(4-Fluoro-phenyl)-2-nitro-propan-1-ol 

Downstream Products

• 672930-43-7 Methyl 4-(4-fluorophenyl)-2,5-dimethyl-3-furoate 
• 444914-20-9 ethyl 4-(4-fluorophenyl)-5-methyl-2-(1-methylethyl)furan-3-carboxylate 
• 1374229-57-8 ethyl 4-(4-fluorophenyl)-2,5-dimethylfuran-3-carboxylate 
• 1374229-56-7 1-[4-(4-fluorophenyl)-2,5-dimethylfuran-3-yl]ethanone 
• 1600521-05-8 1-(4-(4-fluorophenyl)-2,5-dimethyl-1-phenyl-1H-pyrrol-3-yl)ethanone 
• 459-02-9 4-fluoroamphetamine 
• 124401-42-9 1-cyclohexyl-2-isopropyl-4-(4-fluorophenyl)-1H-pyrrole-3-carboxanilide 
• 122223-49-8 1-phenyl-2-isopropyl-4-(4-fluorophenyl)-5-methyl-1H-pyrrole-3-carboxanilide 
• 122223-62-5 4-(4-fluorophenyl)-2-isopropyl-N,1-diphenyl-1H-pyrrole-3-carboxamide 
• 124401-41-8 1,2-diisopropyl-4-(4-fluorophenyl)-1H-pyrrole-3-carboxanilide 

Relevant articles and documents

Substrate promiscuity of ortho-naphthoquinone catalyst: Catalytic aerobic amine oxidation protocols to deaminative cross-coupling and n-nitrosation

ortho-Naphthoquinone-based organocatalysts have been identified as versatile aerobic oxidation catalysts. Primary amines were readily cross-coupled with primary nitroalkanes via deaminative pathway to give nitroalkene derivatives in good to excellent yields. Secondary and tertiary amines were inert to ortho-naphthoquinone catalysts; however, secondary nitroalkanes were readily converted by ortho-naphthoquinone catalysts to the corresponding nitrite species that in situ oxidized the amines to the corresponding N-nitroso compounds. Without using harsh oxidants in a stoichiometric amount, the present catalytic aerobic oxidation protocol utilizes the substrate promiscuity feature to provide a facile access to amine oxidation products under mild reaction conditions.

Dynamic kinetic asymmetric ring-opening/reductive amination sequence of racemic nitroepoxides with chiral amines: Enantioselective synthesis of chiral vicinal diamines

We report a highly diastereoselective synthesis of vicinal diamines by the treatment of nitroepoxides with primary amines and then a reducing agent. When using a chiral primary amine, racemic nitroepoxides are transformed into chiral diamines as a single enantiomers (>95:5 er) through a dynamic kinetic asymmetric transformation (DYKAT). The overall process is a one-pot procedure combining the exposure of nitroepoxides to chiral amines to afford diastereomeric mixtures of aminoimines and subsequent stereoselective imine reduction.

Enzymatic enantiomeric resolution of phenylethylamines structurally related to amphetamine

Both enantiomers of several phenylethylamines, structurally related to amphetamine, have been prepared in good yields and excellent enantiomeric purity by enzymatic kinetic resolution using CAL-B and ethyl methoxyacetate as the acyl donor. In the case of the 4-hydroxyderivative of amphetamine (compound 4i), the S enantiomer racemized possibly in a dynamic kinetic resolution (DKR) under the enzymatic conditions used. The Royal Society of Chemistry 2011.