5910-32-7

Basic information

• Product Name: (2Z)-N-(4-chlorophenyl)-2-cyano-3-[1-(4-fluorobenzyl)-1H-indol-3-yl]prop-2-enamide
• CAS NO: 5910-32-7
• Molecular Formula: C₁₄H₁₂
• Molecular Weight: 429.8734
• Mol File: 5910-32-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 687.3°C at 760 mmHg
• Flash Point: 369.5°C
• Density: 1.25g/cm³
• Vapor Pressure: 9.64E-19mmHg at 25°C
• Refractive Index: 1.629
• CAS DataBase Reference: (2Z)-N-(4-chlorophenyl)-2-cyano-3-[1-(4-fluorobenzyl)-1H-indol-3-yl]prop-2-enamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2Z)-N-(4-chlorophenyl)-2-cyano-3-[1-(4-fluorobenzyl)-1H-indol-3-yl]prop-2-enamide(5910-32-7)
• EPA Substance Registry System: (2Z)-N-(4-chlorophenyl)-2-cyano-3-[1-(4-fluorobenzyl)-1H-indol-3-yl]prop-2-enamide(5910-32-7)

Safety Data

• Hazardous Substances Data: 5910-32-7(Hazardous Substances Data)

Upstream product

• 71870-46-7 1,4,9,10-Tetrahydro-9,10-ethanoanthracene 
• 83143-01-5 9,10-epoxy-1,4,4a,9,9a,10-hexahydroanthracene 
• 573-57-9 1,4-dihydronaphthalene-1,4-epoxide 
• 110-00-9 furan 
• 77-79-2 3-Sulfolene 
• 462-80-6 benzyne 

Downstream Products

• 2141-42-6 1,2,3,4-tetrahydroanthracene 
• 176236-88-7 2,3-epoxy-1,2,3,4-tetrahydroanthracene 
• 1981-38-0 2-phenylanthracene 
• 2026-16-6 2-vinylanthracene 
• 133970-15-7 trans-2-pyrrolidinyl-3-(N-methyl-3',4'-dichlorobenzamido)-1,2,3,4-tetrahydroanthracene 
• 133970-14-6 trans-2-pyrrolidinyl-3-(N-methyl-3',4'-dichlorophenylacetamido)-1,2,3,4-tetrahydroanthracene 
• 7397-92-4 1-bromoanthracene 
• 1101844-20-5 2-(phenylsulfonyl)-1,2-dihydroanthracene 

Relevant articles and documents

Tetraanthra[2,3-b,g,l,q]porphyrin

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A general synthetic method for 2-substituted anthracenes

Anthracenes bearing a primary alkyl, ω-hydroxyalkyl, aryl or vinyl substituent at the 2-position are conveniently prepared by a copper-catalyzed Grignard reaction on 2,3-epoxy-1,2,3,4-tetrahydroanthracene, followed by dehydration - dehydrogenation of the resulting alcohols with tetrachloro-1,2-benzoquinone (o-chloranil).

Synthesis and Properties of 1,1-Dihalogenocyclopropanthracenes

The synthesis of 1,1-difluoro-1H-cyclopropanthracene (3) is described.The key step of the synthesis is the cycloaddition of 1,2-dichloro-3,3-difluorocyclopropene (6) to 2,3-dimethylidene-1,2,3,4-tetrahydronaphthalene (5).The 13C-NMR. spectrum of 3 is assigned on the grounds of C,F-coupling constants, selective H-decoupling and the resulting residual C,H-coupling.The 1,1-dichloro derivative 4 was synthesized by the same route, but could not be isolated pure.Experiments for the reduction to 1H-cyclopropanthracene (2) and for the ionization of 3 or 4 to the cation 16 failed.