1283147-52-3

Basic information

• Product Name: (R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl acrylate
• Synonyms: (R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl acrylate
• CAS NO: 1283147-52-3
• Molecular Weight: 294.304
• Mol File: 1283147-52-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl acrylate(1283147-52-3)
• EPA Substance Registry System: (R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl acrylate(1283147-52-3)

Safety Data

• Hazardous Substances Data: 1283147-52-3(Hazardous Substances Data)

Upstream product

• 54814-41-4 3-(3,4-dimethoxy-phenyl)-2-hydroxy-propionic acid methyl ester 
• 79-10-7 acrylic acid 
• 61871-67-8 3-(3,4-Dimethoxyphenyl)propanal 
• 814-68-6 acryloyl chloride 

Downstream Products

• 1400055-66-4 C₃₄H₃₄O₁₂ 
• 1400055-70-0 C₃₃H₃₂O₁₂ 
• 55757-14-7 (2S,3S)-methyl 2-(3,4-dimethoxyphenyl)-4-((E)-3-(((R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl)oxy)-3-oxoprop-1-en-1-yl)-7-methoxy-2,3-dihydrobenzofuran-3-carboxylate 
• 1310802-43-7 (2R,3R)-methyl 2-(3,4-dimethoxyphenyl)-4-((E)-3-(((R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl)oxy)-3-oxoprop-1-en-1-yl)-7-methoxy-2,3-dihydrobenzofuran-3-carboxylate 
• 868258-16-6 (2S,3S)-4-((E)-3-((R)-1-carboxy-2-(3,4-dimethoxyphenyl)ethoxy)-3-oxoprop-1-en-1-yl)-2-(3,4-dimethoxyphenyl)-7-methoxy-2,3-dihydrobenzofuran-3-carboxylic acid 

Relevant articles and documents

Total synthesis of lithospermic acid using Fe-catalyzed Cross-Dehydrogenative-Coupling reaction and Pd-catalyzed ester-directed C–H olefination

The total synthesis of lithospermic acid has been accomplished employing two C–H activation reactions as key steps. Fe-catalyzed Cross-Dehydrogenative-Coupling reaction was used for the rapid construction of benzofuran framework. Pd-catalyzed ester-direct

Enantioselective total synthesis of (+)-lithospermic acid

An enantioselective synthesis of (+)-lithospermic acid, a potent anti-HIV agent, has been accomplished in a convergent manner in nine steps. The synthesis features an enantioselective intramolecular oxa-Michael addition catalyzed by a quinidine derivative