1220094-19-8

Basic information

• Product Name: (E)-1-formyl-2-[2-(4-methoxyphenyl)ethenyl]benzene
• Synonyms: (E)-1-formyl-2-[2-(4-methoxyphenyl)ethenyl]benzene
• CAS NO: 1220094-19-8
• Molecular Weight: 238.286
• Mol File: 1220094-19-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: (E)-1-formyl-2-[2-(4-methoxyphenyl)ethenyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-formyl-2-[2-(4-methoxyphenyl)ethenyl]benzene(1220094-19-8)
• EPA Substance Registry System: (E)-1-formyl-2-[2-(4-methoxyphenyl)ethenyl]benzene(1220094-19-8)

Safety Data

• Hazardous Substances Data: 1220094-19-8(Hazardous Substances Data)

Upstream product

• 149777-83-3 2-[(E)-2-(4-methoxyphenyl)ethenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 6630-33-7 ortho-bromobenzaldehyde 
• 2591-86-8 N-Formylpiperidine 
• 85676-80-8 (E)-1-bromo-2-[2-(4-methoxyphenyl)ethenyl]benzene 
• 637-69-4 4-Methoxystyrene 

Downstream Products

• 1229445-70-8 (E)-1-(2,2-dibromovinyl)-2-(4-methoxystyryl)benzene 
• 1229445-90-2 (1E)-1-(4-methoxybenzylidene)-2-phenyl-1H-indene 
• 1608154-96-6 2,3-dihydro-4-(4-methoxyphenyl)-2-methyl-1H-2-benzazepine 
• 1323307-77-2 (E)-methyl 3-(2-(4-methoxystyryl)phenyl)-3-hydroxypropanoate 
• 1323307-98-7 (E)-1-(2-(4-methoxystyryl)phenyl)ethanol 
• 1086-43-7 2-(4-methoxyphenyl)-2,3-dihydro-1H-inden-1-one 
• 1323309-21-2 (E)-1-(2-(4-methoxystyryl)phenyl)ethanone 
• 1323307-46-5 (E)-methyl 3-[2-(4-methoxystyryl)phenyl]-3-oxopropanoate 
• 1323308-96-8 2-(4-methoxyphenyl)-1-methylene-1H-indene 
• 207619-53-2 (E)-1-(4-methoxystyryl)-2-vinylbenzene 
• 1195190-00-1 2,3-bis(4-methoxyphenyl)-2,3-dihydro-1H-inden-1-one 

Relevant articles and documents

Phosphazene base-catalyzed hydroamination of aminoalkenes for the construction of isoindoline scaffolds: Application to the total synthesis of aristocularine

A method for isoindoline synthesis via phosphazene base-catalyzed intramolecular hydroamination of aminoalkenes was developed. The reaction has a broad functional group tolerance, including for halide, cyano, and methoxy groups, and could also be used to

Rhodium-catalyzed intramolecular hydroacylation of 1,2-disubstituted alkenes for the synthesis of 2-substituted indanones

The intramolecular hydroacylation of 1,2-disubstituted alkenes was considered to be a challenging task due to the side reactions resulted from the lack of additional substituent at 1-position and the low activity caused by the steric hindrance of substituent at 2-position, and an asymmetric version has not been considered possible due to problems associated with the racemization of the products. We have partially solved these problems. Catalyzed by an activated diphosphine-Rh complex and reacted in a selected dihalogenated solvent, the intramolecular hydroacylation of o-(2-arylvinyl)benzaldehydes provided the corresponding 2-aryl-1-indanones in high yields, and its asymmetric variant using o-(2-alkylvinyl)benzaldehydes afforded chiral 2-alkyl-1-indanones in high yields and with moderate enantioselectivities.

Palladium-Catalyzed Intramolecular Trost–Oppolzer-Type Alder–Ene Reaction of Dienyl Acetates to Cyclopentadienes

A new approach to the synthesis of highly substituted cyclopentadienes, indenes, and cyclopentene-fused heteroarenes by means of the Pd-catalyzed Trost–Oppolzer-type intramolecular Alder–ene reaction of 2,4-pentadienyl acetates is described. This unpreced