92434-54-3

Basic information

• Product Name: Benzene, 1-bromo-2-[2-(4-methoxyphenyl)ethenyl]-
• CAS NO: 92434-54-3
• Molecular Formula: C15H13BrO
• Molecular Weight: 289.172
• Mol File: 92434-54-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 1-bromo-2-[2-(4-methoxyphenyl)ethenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-bromo-2-[2-(4-methoxyphenyl)ethenyl]-(92434-54-3)
• EPA Substance Registry System: Benzene, 1-bromo-2-[2-(4-methoxyphenyl)ethenyl]-(92434-54-3)

Safety Data

• Hazardous Substances Data: 92434-54-3(Hazardous Substances Data)

Upstream product

• 6630-33-7 ortho-bromobenzaldehyde 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 36901-75-4 (2-bromobenzyl)triphenylphosphonium bromide 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 937634-53-2 1-bromo-2-(4-methoxyphenethyl)benzene 
• 937643-47-5 4-(2-bromophenethyl)phenol 
• 27884-09-9 2-(4-methoxyphenyl)benzo[b]thiophene 
• 1608105-74-3 C₁₉H₂₀O₄ 
• 1608105-90-3 C₂₃H₂₀O₄ 
• 1608105-82-3 C₁₇H₁₆O₄ 
• 1608105-38-9 1,1-dimethyl 2-phenyl 2-(2-(4-methoxyphenylethyl)phenyl)ethene-1,1,2-tricarboxylate 
• 1111311-21-7 ethyl 3-(4-methoxybenzyl)-2H-isoindole-1-carboxylate 
• 1111310-64-5 ethyl (Z)-2-hydroxy-2-(2-(4-methoxystyryl)phenyl)acetate 
• 1111310-91-8 ethyl (Z)-2-(2-(4-methoxystyryl)phenyl)-2-(methylsulfonyloxy)acetate 
• 1283153-38-7 1-(4-methoxybenzyl)-2-methyl-1,2-dihydrophthalazine 
• 1283153-07-0 N-(2-(β-4'-methoxystyryl)benzylidene)-N'-methylhydrazine 

Relevant articles and documents

Photochemistry of o-pyrrolylstilbenes and formation of spiro-2H-pyrroles and their rearrangement to dihydroindoles

(Chemical Equation Presented) Excited states of stilbenylpyrroles 1a-1c deactivate by two photochemical processes: cis-trans-isomerization and hydrogen transfer of NH to the stilbene double bond. NH-transfer results in the formation of two quinone dimetha

Palladium(0)-catalyzed arylative dearomatization of phenols

The palladium-catalyzed arylative dearomatization of phenols to yield spirocyclohexadienone products in good to excellent yields has been developed. Preliminary results demonstrate that the formation of the spirocyclic all-carbon quaternary center can be accomplished with high levels of enantiocontrol (up to 91% ee).