149512-01-6

Basic information

• Product Name: Naphthalene, 1,2-dihydro-4-iodo-
• CAS NO: 149512-01-6
• Molecular Formula: C10H9I
• Molecular Weight: 256.086
• Mol File: 149512-01-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Naphthalene, 1,2-dihydro-4-iodo-(CAS DataBase Reference)
• NIST Chemistry Reference: Naphthalene, 1,2-dihydro-4-iodo-(149512-01-6)
• EPA Substance Registry System: Naphthalene, 1,2-dihydro-4-iodo-(149512-01-6)

Safety Data

• Hazardous Substances Data: 149512-01-6(Hazardous Substances Data)

Upstream product

• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 3333-24-2 4-bromo-1,2-dihydronaphthalene 
• 28075-50-5 cyclohex-1-en-1-yl trifluoromethane sulfonate 

Downstream Products

• 1313810-37-5 C₃₀H₄₀O₅Si 
• 1283735-62-5 cyclohexyl(3,4-dihydronaphthalen-1-yl)methanol 
• 1283735-59-0 (3,4-dihydronaphthalen-1-yl)(phenyl)methanol 
• 1190931-42-0 4-(3,4-dihydronaphthalen-1-yl)phenyl ethyl ether 
• 21855-80-1 4-(3,4-dihydronaphthalen-1-yl)phenyl methyl ether 
• 6273-43-4 3,4-dihydro-1-(p-chlorophenyl)naphthalene 
• 6936-14-7 1,2-dihydro-4-(4-methylphenyl)naphthalene 
• 7469-40-1 1-phenyl-3,4-dihydronaphthalene 
• 388-65-8 4-(4-fluorophenyl)-1,2-dihydronaphthalene 
• 21855-82-3 4-(3-methylphenyl)-1,2-dihydronaphthalene 
• 40846-01-3 1-[4-(3,4-dihydronaphthalen-1-yl)phenyl]ethanone 
• 1190931-43-1 4-(3,4-dihydronaphthalen-1-yl)benzaldehyde 
• 107328-74-5 1-(3-methoxyphenyl)-3,4-dihydronaphthalene 
• 52258-16-9 4-methylphenyl 2-naphthyl sulfide 

Relevant articles and documents

Multimetallic Ni- and Pd-Catalyzed Cross-Electrophile Coupling to Form Highly Substituted 1,3-Dienes

The synthesis of highly substituted 1,3-dienes from the coupling of vinyl bromides with vinyl triflates is reported for the first time. The coupling is catalyzed by a combination of (5,5′-bis(trifluoromethyl)-2,2′-bipyridine)NiBr2 and (1,3-bis(diphenylphosphino)propane)PdCl2 in the presence of a zinc reductant. This method affords tetra- and penta-substituted 1,3-dienes that would otherwise be difficult to access and tolerates electron-rich and -poor substituents, heterocycles, an aryl bromide, and a pinacol boronate ester. Mechanistically, the reaction appears to proceed by an unusual zinc-mediated transfer of a vinyl group between the nickel and palladium centers.