632290-89-2

Basic information

• Product Name: ethyl 2-(2-methoxy-4-(prop-1-enyl)phenoxy)acetate
• Synonyms: ethyl 2-(2-methoxy-4-(prop-1-enyl)phenoxy)acetate
• CAS NO: 632290-89-2
• Molecular Weight: 250.295
• Mol File: 632290-89-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 2-(2-methoxy-4-(prop-1-enyl)phenoxy)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(2-methoxy-4-(prop-1-enyl)phenoxy)acetate(632290-89-2)
• EPA Substance Registry System: ethyl 2-(2-methoxy-4-(prop-1-enyl)phenoxy)acetate(632290-89-2)

Safety Data

• Hazardous Substances Data: 632290-89-2(Hazardous Substances Data)

Upstream product

• 51264-70-1 ethyl 2-(4-formyl-2-methoxyphenoxy)acetate 
• 1754-88-7 ethylenetriphenylphosphorane 

Downstream Products

• 1395081-58-9 (S,E)-4-isopropyl-3-(2-(2-methoxy-4-(prop-1-enyl)phenoxy)acetyl)-5,5-diphenyloxazolidin-2-one 
• 1395081-60-3 (S)-3-((2S,3R)-3-(3,4-dimethoxyphenyl)-3-hydroxy-2-(2-methoxy-4-((E)-prop-1-enyl)phenoxy)propanoyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one 
• 1395081-61-4 (S)-3-((2S,3R)-3-hydroxy-2-(2-methoxy-4-((E)-prop-1-enyl)phenoxy)-3-(3,4,5-trimethoxyphenyl)propanoyl)-4-isopropyl-5,5-diphenyloxazolidin-2-one 
• 1395081-63-6 (1R,2R)-1-(3,4-dimethoxyphenyl)-2-(2-methoxy-4-((E)-prop-1-enyl)phenoxy)propane-1,3-diol 
• 1395081-64-7 (1R,2R)-2-(2-methoxy-4-((E)-prop-1-enyl)phenoxy)-1-(3,4,5-trimethoxyphenyl)propane-1,3-diol 
• 1395081-66-9 (2R,3R)-3-(3,4-dimethoxyphenyl)-3-hydroxy-2-(2-methoxy-4-((E)-prop-1-enyl)phenoxy)propyl-4-methylbenzenesulfonate 
• 1395081-67-0 (2R,3R)-3-hydroxy-2-(2-methoxy-4-((E)-prop-1-enyl)phenoxy)-3-(3,4,5-trimethoxyphenyl)propyl 4-methylbenzenesulfonate 
• 1395081-54-5 C₁₄H₁₈O₄ 
• 7510-46-5 (E)-2-(2-methoxy-4-(prop-1-enyl)phenoxy)acetic acid 

Relevant articles and documents

A concise asymmetric synthesis of (-)-virolin, (-)-surinamensin,(-)- raphidecursinol B and (-)-polysphorin

Highly concise and general asymmetric syntheses of biologically important natural (-)-8,4-oxyneolignans [(-)-virolin, (-)-surinamensin, (-)-raphidecursinol B, and (-)-polysphorin] are reported. The key step in the synthesis is the Evan's syn-aldol reaction to achieve the adducts with the desired stereochemistry. The four biologically important plant metabolites were synthesized using two common intermediates. Georg Thieme Verlag Stuttgart · New York.