93340-46-6

Basic information

• Product Name: 2-Propenoic acid, 3-(4-methoxyphenyl)-, phenyl ester
• Synonyms: phenyl trans-p-methoxycinnamate;4-Methoxy-trans-zimtsaeure-phenylester;phenyl 4-methoxycinnamate;4-methoxy-trans-cinnamic acid phenyl ester
• CAS NO: 93340-46-6
• Molecular Formula: C16H14O3
• Molecular Weight: 254.285
• Mol File: 93340-46-6.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 3-(4-methoxyphenyl)-, phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-(4-methoxyphenyl)-, phenyl ester(93340-46-6)
• EPA Substance Registry System: 2-Propenoic acid, 3-(4-methoxyphenyl)-, phenyl ester(93340-46-6)

Safety Data

• Hazardous Substances Data: 93340-46-6(Hazardous Substances Data)

Upstream product

• 1963-36-6 4-methoxycinnamaldehyde 
• 108-95-2 phenol 
• 696-62-8 para-iodoanisole 
• 937-41-7 phenyl acrylate 
• 943-89-5 (E)-3-(4-methoxyphenyl)acrylic acid 
• 1885-14-9 phenyl chloroformate 
• 34446-64-5 (E)-3-(4-methoxyphenyl)propenoyl chloride 
• 830-09-1 3-(4'-methoxyphenyl)propenoic acid 
• 42996-84-9 p-methoxycinnamoyl chloride 

Downstream Products

• 14482-11-2 (E)-p-methoxycinnamonitrile 
• 149777-83-3 2-[(E)-2-(4-methoxyphenyl)ethenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 71907-23-8 2‐[(E)‐2‐(4‐methoxyphenyl)ethenyl]‐1,3‐benzoxazole 
• 1221005-30-6 (2E)-N-{[2-(4-hydroxybenzylidene)hydrazino](imino)methyl}-3-(4-methoxyphenyl)acrylamide 
• 1221005-35-1 (2E)-N-{[2-(4-fluorobenzylidene)hydrazino](imino)methyl}-3-(4-methoxyphenyl)acrylamide 
• 1221005-43-1 (2E)-N-{[2-(3,4,5-trimethoxybenzylidene)hydrazino](imino)methyl}-3-(4-methoxyphenyl)acrylamide 
• 1221005-40-8 (2E)-N-{[2-(3,4-dimethoxybenzylidene)hydrazino](imino)methyl}-3-(4-methoxyphenyl)acrylamide 
• 32140-83-3 4-(4-methoxyphenyl)-3,4-dihydrocoumarin 
• 1694-19-5 E-1-(phenyl)-2-(4'-methoxyphenyl)ethene 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 4705-34-4 1,2-bis(4-methoxyphenyl)ethene 

Relevant articles and documents

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Method of coupling, and the coupling method using the aromatic group-substituted heterocyclic compound

Provided is an easy method (coupling method) capable of easily synthesizing a compound group in which aromatic molecules and aromatic molecules are coupled, a compound group in which aromatic molecules and alkene molecules are coupled, and the like without producing halogen waste and without the need to use scarce and expensive palladium. A compound (A) shown by general formula (A): Ar-H and a compound (B1) shown by general formula (B1): RaOCO-Ar', a compound (B2) shown by general formula (B2): RbCH=C(Ar")2, or a compound (B3) shown by general formula (B3): RcOCOCH=C(Ar")2 are reacted in the presence of a nickel compound.

Dinuclear zinc catalyzed asymmetric spirannulation reaction: An umpolung strategy for formation of α-alkylated-α-hydroxyoxindoles

A highly diastereo- and enantioselective formal [3 + 2] cycloaddition of α,β-unsaturated esters and 3-hydroxyoxindoles catalyzed by a dinuclear zinc-ProPhenol complex is reported. The stereoselective Michael additions of 3-hydroxyoxindoles and the subsequent transesterifications afford spirocyclic δ-lactones.