1094496-64-6

Basic information

• Product Name: (R)-1-(furan-2-yl)-4-nitro-3-phenylbutan-1-one
• Synonyms: (R)-1-(furan-2-yl)-4-nitro-3-phenylbutan-1-one
• CAS NO: 1094496-64-6
• Molecular Weight: 259.262
• Mol File: 1094496-64-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-1-(furan-2-yl)-4-nitro-3-phenylbutan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-1-(furan-2-yl)-4-nitro-3-phenylbutan-1-one(1094496-64-6)
• EPA Substance Registry System: (R)-1-(furan-2-yl)-4-nitro-3-phenylbutan-1-one(1094496-64-6)

Safety Data

• Hazardous Substances Data: 1094496-64-6(Hazardous Substances Data)

Upstream product

• 1192-62-7 1-(2-furyl)-1-ethanone 
• 102-96-5 (2-nitroethenyl)benzene 
• 75-52-5 nitromethane 
• 3988-74-7 (E)-1-(furan-2-yl)-3-phenylprop-2-en-1-one 
• 1777-60-2 [(furan-2-ylcarbonyl)methylene]triphenylphosphorane 
• 100-52-7 benzaldehyde 

Relevant articles and documents

High pressure-assisted low-loading asymmetric organocatalytic conjugate addition of nitroalkanes to chalcones

The application of high pressure (up to 9 kbar) allows for relatively fast (1-5 h) and highly enantioselective 1,4-addition of nitromethane and 2-nitropropane to chalcones at room temperature with substantial reduction of catalyst loading (0.2-1 mol% of cinchona alkaloid-based thioureas and squaramides). Various γ-nitroketones were obtained at 9 kbar with high yield and enantioselectivity (up to 98%), whereas in control experiments at atmospheric pressure usually only a small amount (10%) of products were formed after 20 h.