104129-40-0

Upstream product

• 615-90-7 2,5-dimethylhydroquinone 
• 4962-28-1 2,5-dimethyl-4-methoxyphenol 
• 2674-32-0 1,4-dimethoxy-2,5-dimethylbenzene 

Downstream Products

• 854838-12-3 (2,5-dimethoxy-3,6-dimethyl-benzylidene)-malonic acid 
• 855272-72-9 1-(2,5-dimethoxy-3,6-dimethyl-phenyl)-ethanol 
• 163520-28-3 2,5-dimethoxy-3,6-dimethylphenol 
• 180777-94-0 (E)-3-[4-(n-heptyloxy)-2,5-dimethoxy-3,6-dimethylphenyl]-2-[5-(3-pyridyl)pentyl]-2-propenoic acid 
• 144562-71-0 ethyl (E)-3-(2,4,5-trimethoxy-3,6-dimethylphenyl)-2-[6-(3-pyridyl)hexyl]-2-propenoate 
• 144562-77-6 2-[1-(4-Ethoxy-2,5-dimethoxy-3,6-dimethyl-phenyl)-meth-(E)-ylidene]-7-pyridin-3-yl-heptanoic acid ethyl ester 
• 144562-59-4 ethyl (E)-3-(2,4,5-trimethoxy-3,6-dimethylphenyl)-2-[5-(pyridin-3-yl)pentyl]-2-propenoate 
• 144562-89-0 (E)-3-(2,4,5-trimethoxy-3,6-dimethylphenyl)-2-[6-(3-pyridyl)hexyl]-2-propenoic acid 
• 144562-94-7 (E)-3-(4-ethoxy-2,5-dimethoxy-3,6-dimethylphenyl)-2-[5-(3-pyridyl)pentyl]-2-propenoic acid 
• 144562-70-9 6-Pyridin-3-yl-2-[1-(2,4,5-trimethoxy-3,6-dimethyl-phenyl)-meth-(E)-ylidene]-hexanoic acid ethyl ester 
• 144562-60-7 (E)-3-(2,4,5-Trimethoxy-3,6-dimethylphenyl)-2-[5-(pyridin-3-yl)pentyl]-2-propenoic acid 
• 144562-68-5 5-Pyridin-3-yl-2-[1-(2,4,5-trimethoxy-3,6-dimethyl-phenyl)-meth-(E)-ylidene]-pentanoic acid ethyl ester 
• 144562-88-9 (E)-3-(2,4,5-trimethoxy-3,6-dimethylphenyl)-2-[4-(3-pyridyl)butyl]-2-propenoic acid 
• 144562-86-7 (E)-3-(2,4,5-trimethoxy-3,6-dimethylphenyl)-2-[3-(3-pyridyl)propyl]-2-propenoic acid 

Relevant academic research and scientific papers

Photoactivation of amino-substituted 1,4-benzoquinones for release of carboxylate and phenolate leaving groups using visible light

Upon exposure to visible light, 2-pyrrolidino-substituted 3,6-dimethyl-1,4-benzoquinones photocyclize to give benzoxazolines with quantum yields of 0.07-0.10 in CH2Cl2, 0.02-0.04 in CH 3CN, and 3/su

Photochemical cyclization with release of carboxylic acids and phenol from pyrrolidino-substituted 1,4-benzoquinones using visible light

(Chemical Equation Presented) Visible light irradiation of 5-acyloxymethyl- and 5-phenoxymethyl-2-pyrrolidino-1,4-benzoquinones effects photoisomerization to labile oxazolidines, which undergo elimination of carboxylate or phenolate leaving groups in high