16623-96-4

Upstream product

• 73314-69-9 methoxymethylenecyclododecane 
• 950-33-4 Cyclododecanone dimethoxy acetal 

Downstream Products

• 830-13-7 cyclododecanone 
• 229323-98-2 N 89 
• 410085-00-6 1-[6-(2-tetrahydropyranyloxy)hexyldioxy]cyclododecyl hydroperoxide 
• 410085-01-7 1-[(3-butenyl)dioxy]cyclododecyl hydroperoxide 
• 504396-48-9 1-[(2-propenyl)dioxy]cyclododecyl hydroperoxide 
• 601493-85-0 1-[(5-hexenyl)dioxy]cyclododecyl hydroperoxide 
• 601493-84-9 1-[(4-pentenyl)dioxy]cyclododecyl hydroperoxide 
• 370879-26-8 1,1'-cyclododecylidenebis[(3-methyl-3-butenyl)peroxide] 
• 410084-96-7 1-(butyldioxy)cyclododecyl hydroperoxide 
• 1018495-72-1 3-methyl-3-cyclohexyl-1,2,4,5-tetraoxa-3-silaspiro[5.11]heptadecane 
• 1018495-73-2 3,3-diphenyl-1,2,4,5-tetraoxa-3-silaspiro[5.11]heptadecane 
• 1097634-97-3 1-hydroperoxy-1-(1-methoxycyclohexylperoxy)cyclododecane 
• 40832-73-3 N-(4-chlorophenyl)piperidine 
• 1427511-77-0 1,1-bis(2-octylperoxy)cyclododecane 

Relevant academic research and scientific papers

Synthesis and antimalarial activity of novel medium-sized 1,2,4,5-tetraoxacycloalkanes

CsOH- or Ag2O-mediated cycloalkylation of (alkylidene)bisperoxides 3 and 1,n-dihaloalkanes (n = 3-8) provided the corresponding medium-sized 1,2,4,5-tetraoxacycloalkanes 4-8 in moderate yields. Subsequent evaluation of the antimalarial activity of the cyclic peroxides 4-8 in vitro and in vivo revealed that 1,2,6,7-tetraoxaspiro[7.11]nonadecane 4a has considerable potential as a new, inexpensive, and potent antimalarial drug.

A New Method for the Synthesis of gem-Dihydroperoxides

The tungstic acid-catalysed reaction of ketals with hydrogen peroxide provides a convenient and efficient method for preparing gem-dihydroperoxides.