1415560-39-2

Basic information

• Product Name: (S,E)-2-(1,3-diphenylallyl)-5-methoxyphenol
• Synonyms: (S,E)-2-(1,3-diphenylallyl)-5-methoxyphenol
• CAS NO: 1415560-39-2
• Molecular Weight: 316.4
• Mol File: 1415560-39-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S,E)-2-(1,3-diphenylallyl)-5-methoxyphenol(CAS DataBase Reference)
• NIST Chemistry Reference: (S,E)-2-(1,3-diphenylallyl)-5-methoxyphenol(1415560-39-2)
• EPA Substance Registry System: (S,E)-2-(1,3-diphenylallyl)-5-methoxyphenol(1415560-39-2)

Safety Data

• Hazardous Substances Data: 1415560-39-2(Hazardous Substances Data)

Upstream product

• 1415560-26-7 C₁₆H₁₈O₃ 
• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 
• 926236-29-5 2-hydroxy-4-methoxybenzhydrol 
• 150-19-6 O-methylresorcine 
• 100-52-7 benzaldehyde 
• 6783-05-7 trans-2-phenylvinylboronic acid 
• 536-74-3 phenylacetylene 

Downstream Products

• 1415560-52-9 C₁₆H₁₆O₂ 
• 2543-95-5 (S)-(-)-4-methoxydalbergione 
• 1415560-56-3 (S)-2-(2,4-dimethoxyphenyl)-2-phenylacetaldehyde 
• 251317-26-7 (S)-3-(2',4'-dimethoxyphenyl)-3-phenyl-1-propene 
• 163686-11-1 (S)-3-(2,4-dimethoxyphenyl)-3-phenylpropan-1-ol 
• 1415560-49-4 C₂₃H₂₂O₂ 

Relevant articles and documents

Enantioselective Multicomponent Condensation Reactions of Phenols, Aldehydes, and Boronates Catalyzed by Chiral Biphenols

Chiral diols and biphenols catalyze the multicomponent condensation reaction of phenols, aldehydes, and alkenyl or aryl boronates. The condensation products are formed in good yields and enantioselectivities. The reaction proceeds via an initial Friedel-Crafts alkylation of the aldehyde and phenol to yield an ortho-quinone methide that undergoes an enantioselective boronate addition. A cyclization pathway was discovered while exploring the scope of the reaction that provides access to chiral 2,4-diaryl chroman products, the core of which is a structural motif found in natural products.