84952-10-3

Upstream product

• 109-65-9 1-bromo-butane 
• 611-99-4 4,4'-Dihydroxybenzophenone 
• 1126-79-0 n-butyl phenyl ether 
• 79-37-8 oxalyl dichloride 
• 1248384-02-2 C₃₀H₃₉InO₃ 
• 1239896-49-1 C₃₀H₃₉BiO₃ 

Downstream Products

• 111825-33-3 1,1-bis-(4-butoxy-phenyl)-ethene 
• 103510-05-0 1,1-bis-(4-butoxy-phenyl)-4,4-bis-(4-methoxy-phenyl)-buta-1,3-diene 
• 103567-19-7 1,1,4,4-tetrakis-(4-butoxy-phenyl)-buta-1,3-diene 

Relevant academic research and scientific papers

Dinuclear metallocene compound, catalyst composition and method for preparing olein polymer using the same

The present invention relates to a dinuclear metallocene compound, a catalyst compound, and a method for manufacturing an olefin polymer using the same. An embodiment of the present invention provides the dinuclear metallocene compound represented by chem

Photochemical site-selective synthesis of [70]methanofullerenes

Methanofullerenes such as the well-known [70]PCBM are commonly synthesized under harsh conditions to obtain the product as a mixture of site-isomers (namely α, β and minor γ) due to the D5h symmetry of the C70 cage. We report the fir

Reaction of diazocompounds with C70: unprecedented synthesis and characterization of isomeric [5,6]-fulleroids

The synthesis of a variety of PCBM-type [5,6]-fulleroids and their further highly selective photoisomerization to the respective [6,6]-methanofullerenes is presented. Interestingly, the chemical reactivity of [5,6]-fulleroids reveals the same trend (a > b

Oxalyl chloride as carbonyl synthon in Pd-catalyzed carbonylations of triarylbismuth and triarylindium organometallic nucleophiles

Oxalyl chloride has been demonstrated to function as C1 carbonyl synthon in the carbonylations of triarylbismuth and triarylindium nucleophiles under palladium-catalyzed conditions. All the three aryl groups from both bismuth and indium reagents participated in carbonylative couplings to afford the corresponding functionalized ketones in high yields. This study also disclosed a novel utilization of oxalyl chloride as facile alternative source of CO for carbonylations under palladium catalysis.