1173280-41-5

Basic information

• Product Name: 6-methoxy-2-[2-(4-methylphenyl)-(E)-ethenyl]-naphthalene
• Synonyms: 6-methoxy-2-[2-(4-methylphenyl)-(E)-ethenyl]-naphthalene
• CAS NO: 1173280-41-5
• Molecular Weight: 274.362
• Mol File: 1173280-41-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-methoxy-2-[2-(4-methylphenyl)-(E)-ethenyl]-naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 6-methoxy-2-[2-(4-methylphenyl)-(E)-ethenyl]-naphthalene(1173280-41-5)
• EPA Substance Registry System: 6-methoxy-2-[2-(4-methylphenyl)-(E)-ethenyl]-naphthalene(1173280-41-5)

Safety Data

• Hazardous Substances Data: 1173280-41-5(Hazardous Substances Data)

Upstream product

• 1192578-74-7 (E)-2-methoxy-6-(2-methoxyvinyl)naphthalene 
• 380481-66-3 5,5-dimethyl-2-(4-methylphenyl)-1,3,2-dioxaborinane 
• 3453-33-6 6-methoxynaphthalene-2-carbaldehyde 
• 2378-86-1 4-methylbenzyltriphenylphosphonium bromide 

Downstream Products

• 1173280-58-4 6-methoxy-2-[2-(4-bromomethyl-phenyl)-(E)-ethenyl]-naphthalene 

Relevant articles and documents

Highly E-Selective, Stereoconvergent Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling of Alkenyl Ethers

An improved method for the nickel-catalyzed Suzuki-Miyaura cross-coupling of alkenyl ethers is reported. This stereoconvergent protocol allows for the utilization of a wide range of alkenyl ethers and aryl boronic esters for the synthesis of variously sub

Studies toward the photochemical synthesis of functionalized [5]- and [6] carbohelicenes

(Chemical Equation Presented) An efficient route to nonsymmetrical helical menthyl esters by means of an oxidative photocyclization reaction of dissymmetric bis-stilbenes is reported. The developed route allows the introduction of functionality on rings A, E, or F, and the influence of the substituent pattern on the photochemical reaction has been examined. Diastereoselectivity is observed when a double chiral induction strategy with dimenthyl helicene esters synthesized in a 70:30 ratio of isomers is used.