195451-92-4

Upstream product

• 2009-83-8 6-chloro-1-hexanol 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 738604-45-0 [(6-iodohexyl)oxy](tert-butyl)diphenylsilane 
• 352459-89-3 4-benzenesulfonyl-1,11-bis-(tert-butyl-diphenyl-silanyloxy)-5-methoxymethoxymethyl-undecan-3-ol 
• 352459-87-1 (8-benzenesulfonyl-7-methoxymethoxymethyl-octyloxy)-tert-butyl-diphenyl-silane 
• 352459-85-9 tert-butyl-(7-iodomethyl-8-methoxymethoxy-octyloxy)-diphenyl-silane 
• 352459-82-6 8-(tert-butyl-diphenyl-silanyloxy)-2-methoxymethoxymethyl-octan-1-ol 
• 352459-80-4 2-[6-(tert-butyl-diphenyl-silanyloxy)-hexyl]-propane-1,3-diol 
• 441787-81-1 9-[6-(tert-butyldiphenylsilyloxy)hexyl]carbazole 
• 352459-77-9 2-[6-(tert-butyl-diphenyl-silanyloxy)-hexyl]-malonic acid diethyl ester 

Relevant academic research and scientific papers

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.

Efficient fully functionalized photorefractive polymethacrylates with infrared sensitivity and different spacer lengths

A series of photorefractive polymethacrylates, containing a Disperse Red type chromophore and carbazole as charge transport agent with various spacer lengths, was synthesized and characterized. The photorefractive effect of these materials was studied by

Synthesis of 5-(mercaptomethyl)-3(E)-undecene-1,11-dioic acid, a non-peptide glutathione analog

The key step in the synthesis of the title compound is a Julia reaction to create the E-double bond by introducing a functionalized C3 carbon chain.