490-19-7

Upstream product

• 103-26-4 Methyl cinnamate 
• 7647-01-0 hydrogenchloride 
• 2898-38-6 6,7-diphenyl-3-oxabicyclo[3.1.1]heptane-2,4-dione 
• 490-17-5 2,4-diphenyl-cyclobutane-1,3-dicarboxylic acid bis-(2-methoxycarbonyl-tropan-3-yl ester) 
• 109212-92-2 (+/-)-γ-truxillic acid monoamide 
• 64-19-7 acetic acid 
• 109212-92-2 (+)-γ-truxillic acid monoamide 
• 109212-92-2 (-)-γ-truxillic acid monoamide 
• 67-56-1 methanol 
• 621-82-9 Cinnamic acid 
• 17916-52-8 α-truxillic acid dichloride 
• 2898-38-6 γ-truxillic anhydride 

Downstream Products

• 56280-73-0 2,4-diphenyl-cyclobutane-1,3-dicarboxylic acid diethyl ester 
• 490-20-0 truxillic acid 
• 124-38-9 carbon dioxide 
• 65-85-0 benzoic acid 
• 17916-52-8 γ-truxillic acid chloride 
• 2898-38-6 γ-truxillic anhydride 
• 621-82-9 Cinnamic acid 
• 109249-55-0 2c,4t-bis-(4-nitro-phenyl)-cyclobutane-1r,3t-dicarboxylic acid 
• 2898-38-6 6,7-diphenyl-3-oxabicyclo[3.1.1]heptane-2,4-dione 
• 528-38-1 ε-truxillic acid 
• 17916-52-8 α-truxillic acid dichloride 
• 140-10-3 (E)-3-phenylacrylic acid 
• 2904-91-8 α-truxillic acid dimethylester 

Relevant academic research and scientific papers

Electrochemical methoxylation of cinnamic acid and its derivatives

Electrochemical methoxylation of cinnamic acid is accompanied by decarboxylation and yields 1,1,2-trimethoxy-2-phenylethane through formation of γ-truxillic acid in the initial stage. Under the same conditions methyl cinnamate and cinnamamide give rise to

Regioselective photodimerization of cinnamic acid in a micellar solution

Irradiation of trans-cinnamic acid (1) and its methyl ester (2) in 1% aq. cetyltirmethylammonium bromide gave dimeric products in 35 and 29% yields as a mixture of truxinic and truuxillic acids in a ratio of 19 : 1 and 3.8 : 1, respectively, while in homogeneous solutions (1) gave no photodimers and (2) gave dimeric products in 2.3% yield under similar reaction conditions.