51686-50-1

Basic information

• Product Name: methyl 3-(2,3,4-trimethoxybenzoyl)propionate
• Synonyms: methyl 3-(2,3,4-trimethoxybenzoyl)propionate
• CAS NO: 51686-50-1
• Molecular Weight: 282.293
• Mol File: 51686-50-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 3-(2,3,4-trimethoxybenzoyl)propionate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-(2,3,4-trimethoxybenzoyl)propionate(51686-50-1)
• EPA Substance Registry System: methyl 3-(2,3,4-trimethoxybenzoyl)propionate(51686-50-1)

Safety Data

• Hazardous Substances Data: 51686-50-1(Hazardous Substances Data)

Upstream product

• 108-30-5 succinic acid anhydride 
• 634-36-6 1,2,3-trimethoxybenzene 
• 77-78-1 dimethyl sulfate 
• 3878-55-5 methyl hydrogen succinate 

Downstream Products

• 51686-51-2 methyl 4-(2,3,4-trimethoxyphenyl)butanoate 
• 74994-52-8 Acetic acid 1-[2-(4-methoxy-phenyl)-ethyl]-5-(2,3,4-trimethoxy-phenyl)-pentyl ester 
• 74882-24-9 1-(4-Methoxy-phenyl)-7-(2,3,4-trimethoxy-phenyl)-heptan-3-one 
• 74994-46-0 (+/-)-1-(4-methoxyphenyl)-7-(2,3,4-trimethoxyphenyl)heptan-3-ol 
• 56438-60-9 2-[2-(4-methoxyphenyl)ethyl]-1,3-dithiane 
• 74882-28-3 2-[2-(4-Methoxy-phenyl)-ethyl]-2-[4-(2,3,4-trimethoxy-phenyl)-butyl]-[1,3]dithiane 
• 74882-11-4 Toluene-4-sulfonic acid 4-(2,3,4-trimethoxy-phenyl)-butyl ester 
• 74882-21-6 1-(2,3,4-trimethoxyphenyl)butane 
• 74882-10-3 4-(2,3,4-trimethoxyphenyl)-1-bromobutane 
• 74882-09-0 4-(2,3,4-trimethoxyphenyl)butan-1-ol 
• 5406-18-8 3-(p-methoxyphenyl)-1-propanol 
• 20401-88-1 3-(4-methoxyphenyl)propional 
• 74882-22-7 C₂₆H₃₈O₆ 
• 51686-52-3 4-(2,3,4-trimethoxy-phenyl)-butyric acid 

Relevant articles and documents

Novel conformationally restricted tetracyclic analogs of δ8- tetrahydrocannabinol

Novel analogs of (-)-Δ8-tetrahydrocannabinol (Δ8-THC) in which the conformation of the side chain was restricted by incorporating the first one or two carbons into a six membered ring fused with the aromatic phenolic A ring were synt

Methods for the Construction of Linear 1,7-Diarylheptanoids; Synthesis of Di-O-methylcentrolobol and Precursors (Synthetic and Biosynthetic) to the meta,meta-Bridged Biphenyls Myricanol and Myricanone

1,7-diarylheptanoids are a varied natural product class in which 'linear' types appear to be biosynthetic precursors to macro(carbo)cyclic (3), macro(oxa)cyclic (4), and condensed polycyclic (5) examples.Various methods (suitable for radiolabelling) are described for constructing 'linear' diarylheptanoids, including Grignard couplings (employing activated magnesium) with arylpropanals and oxazonium salts (11a), (11h), (15a), and (15b)> and dithian alkylation (15c)>.Alkyl-lithium treatment of the benzyloxydithian (19b) gave 1,2,3-triphenylcyclopropane.Syntheses via trialkylcyanoborates were frustrated by disproportionation of the intermediate trialkylboranes.The diarylheptanoids synthesised (11a-h) and (15a-e) include synthetic and biosynthetic precursors to meta,meta-bridged biphenyls and related macrocyclic ethers.