107228-95-5

Upstream product

• 21244-13-3 7-(4'-methoxyphenyl)heptanoic acid 
• 6294-17-3 1-bromo-6-chlorohexane 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 1186136-94-6 1-(6-chlorohexyl)-4-methoxybenzene 
• 124-38-9 carbon dioxide 
• 64431-79-4 4-(6-bromohexyl)phenol 
• 21244-11-1 7-(4-methoxy-phenyl)-7-oxo-heptanoic acid 

Downstream Products

• 107298-62-4 Acetic acid 4-{7-[7-(4-acetoxy-cyclohexyl)-heptanoylperoxy]-7-oxo-heptyl}-cyclohexyl ester 
• 107228-86-4 Acetic acid 4-{7-[7-(4-acetoxy-cyclohexyl)-heptanoylperoxy]-7-oxo-heptyl}-cyclohexyl ester 
• 107228-80-8 Acetic acid 4-[6-(4,5-dimethoxy-2-methyl-3,6-dioxo-cyclohexa-1,4-dienyl)-hexyl]-cyclohexyl ester 
• 107228-78-4 Acetic acid 4-[6-(4,5-dimethoxy-2-methyl-3,6-dioxo-cyclohexa-1,4-dienyl)-hexyl]-cyclohexyl ester 
• 107228-81-9 cis-6-<6-(4-hydroxycyclohexyl)hexyl>-2,3-dimethoxy-5-methyl-1,4-benzoquinone 
• 107228-79-5 trans-6-<6-(4-hydroxycyclohexyl)hexyl>-2,3-dimethoxy-5-methyl-1,4-benzoquinone 
• 116460-86-7 cis-7-(4-acetoxycyclohexyl)heptanoic acid 
• 107228-90-0 trans-7-(4-acetoxycyclohexyl)heptanoic acid 
• 107228-84-2 bis<7-(4-acetoxyphenyl)heptanoyl> peroxide 
• 107228-72-8 6-<6-(4-acetoxyphenyl)hexyl>-2,3-dimethoxy-5-methyl-1,4-benzoquinone 
• 107228-73-9 6-<6-(4-hydroxyphenyl)hexyl>-2,3-dimethoxy-5-methyl-1,4-benzoquinone 
• 116460-84-5 Acetic acid 4-(6-chlorocarbonyl-hexyl)-phenyl ester 
• 107228-92-2 trans-7-(4-hydroxycyclohexyl)heptanoic acid 
• 107228-94-4 cis-7-(4-hydroxycyclohexyl)heptanoic acid 

Relevant academic research and scientific papers

Ni-catalyzed carboxylation of unactivated primary alkyl bromides and sulfonates with CO2

A Ni-catalyzed carboxylation of unactivated primary alkyl bromides and sulfonates with CO2 at atmospheric pressure is described. The method is characterized by its mild conditions and remarkably wide scope without the need for air- or moisture-sensitive reagents, which make it a user-friendly and operationally simple protocol en route to carboxylic acids.

Ni-Catalyzed Carboxylation of Unactivated Alkyl Chlorides with CO2

A catalytic carboxylation of unactivated primary, secondary, and tertiary alkyl chlorides with CO2 at atmospheric pressure is described. This protocol represents the first intermolecular cross-electrophile coupling of unactivated alkyl chlorides, thus leading to new knowledge in the cross-coupling arena.

Organic materials with nonlinear optical properties

The present invention is directed to organic materials that have the ability to double or triple the frequency of light that is directed through the materials. Particularly, the present invention is directed to the compound 4-[4-(2R)-2-cyano-7-(4'-pentylo