239089-25-9

Basic information

• Product Name: 5,5-Bis(p-methoxybenzyloxymethyl)-2,2-dimethyl-1,3-dioxane
• Synonyms: 5,5-Bis(p-methoxybenzyloxymethyl)-2,2-dimethyl-1,3-dioxane
• CAS NO: 239089-25-9
• Molecular Weight: 416.514
• Mol File: 239089-25-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 5,5-Bis(p-methoxybenzyloxymethyl)-2,2-dimethyl-1,3-dioxane(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5-Bis(p-methoxybenzyloxymethyl)-2,2-dimethyl-1,3-dioxane(239089-25-9)
• EPA Substance Registry System: 5,5-Bis(p-methoxybenzyloxymethyl)-2,2-dimethyl-1,3-dioxane(239089-25-9)

Safety Data

• Hazardous Substances Data: 239089-25-9(Hazardous Substances Data)

Upstream product

• 770-74-1 2,2-dimethyl-5,5-bis(hydroxymethyl)-1,3-dioxane 
• 824-94-2 p-methoxybenzyl chloride 
• 20605-01-0 diethyl bis(hydroxymethyl)malonate 
• 51335-75-2 2,2-Dimethyl-1,3-dioxacyclohexane-5,5-dicarboxylic acid,diethyl ester 

Downstream Products

• 239089-27-1 9-(4-methoxyphenyl)-3,3-dimethyl-2,4,8,10-tetraoxaspiro[5.5]undecane 
• 239089-26-0 (5-(((4-methoxybenzyl)oxy)methyl)-2,2-dimethyl-1,3-dioxan-5-yl)methanol 
• 239089-28-2 5-Formyl-5-p-methoxybenzyloxymethyl-2,2-dimethyl-1,3-dioxane 
• 239089-29-3 (1'R)-5-(1'-Hydroxybut-3'-enyl)-5-p-methoxybenzyloxymethyl-2,2-dimethyl-5-(1'-trimethylsilyloxybut-3'-enyl)-1,3-dioxane 
• 239089-32-8 (1'R,3'S)-5-{1',3'-Dihydroxy-3'-[furan-2''(5''H)-on-4''-yl]propyl}-5-p-methoxybenzyloxymethyl-2,2-dimethyl-1,3-dioxane 
• 239089-40-8 (1'R,3'R)-5-{1',3'-Dihydroxy-3'-[furan-2''(5''H)-on-4''-yl]propyl}-5-p-methoxybenzyloxymethyl-2,2-dimethyl-1,3-dioxane 
• 239089-33-9 (1'R,3'S)-5-{1',3'-Bistriethylsilyloxy-3'-[furan-2''(5''H)-on-4''-yl]propyl}-5-p-methoxybenzyloxymethyl-2,2-dimethyl-1,3-dioxane 

Relevant articles and documents

Synthetic studies on azadirachtin: Construction of the highly functionalized decalin moiety of azadirachtin

Construction of the left segment of azadirachtin in naturally occurring enantiomer is described. The key reaction is an intramolecular Diels-Alder reaction, which was performed under thermal conditions to afford the highly functionalized decalin compounds selectively.