871809-95-9

Basic information

• Product Name: (R)-4-benzyloxy-6-(4-benzyloxyphenyl)hexan-2-one
• Synonyms: (R)-4-benzyloxy-6-(4-benzyloxyphenyl)hexan-2-one
• CAS NO: 871809-95-9
• Molecular Weight: 388.507
• Mol File: 871809-95-9.mol

Chemical Properties

• CAS DataBase Reference: (R)-4-benzyloxy-6-(4-benzyloxyphenyl)hexan-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-4-benzyloxy-6-(4-benzyloxyphenyl)hexan-2-one(871809-95-9)
• EPA Substance Registry System: (R)-4-benzyloxy-6-(4-benzyloxyphenyl)hexan-2-one(871809-95-9)

Safety Data

• Hazardous Substances Data: 871809-95-9(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 68486-77-1 3-(4-(benzyloxy)phenyl)propanal 
• 871809-93-7 (+)-(3R)-1-[4-(benzyloxy)phenyl]hex-5-en-3-ol 
• 871809-94-8 (R)-4-benzyloxy-6-(4-benzyloxyphenyl)hex-1-ene 

Downstream Products

• 913814-42-3 1-benzyloxy-4-[(3R,5R,7R)-3-benzyloxy-5,7-bis(tert-butyldimethylsilyloxy)eicosyl]benzene 
• 913814-43-4 4-[(3R,5R,7R)-5,7-bis(tert-butyldimethylsilyloxy)-3-hydroxyeicosyl]phenol 
• 913814-44-5 (5S,7R)-5,7-di[1-(tert-butyl)-1,1-dimethylsilyl]oxy-1-(4-hydroxyphenyl)icosan-3-one 
• 913814-41-2 (4R,6R)-4-[(R)-2-benzyloxy-4-(4-benzyloxyphenyl)butyl]-2,2-dimethyl-6-n-tridecyl-[1,3]dioxane 
• 913814-40-1 (3R,5S,7R)-3-benzyloxy-1-(4-benzyloxyphenyl)eicosane-5,7-diol 
• 871809-97-1 (4S,6R)-4-[(R)-2-benzyloxy-4-(4-benzyloxyphenyl)butyl]-2,2-dimethyl-6-n-tridecyl-[1,3]dioxane 
• 871809-99-3 (4S,6R)-4-[(R)-2-hydroxy-4-(4-hydroxyphenyl)butyl]-2,2-dimethyl-6-n-tridecyl-[1,3]dioxane 
• 913814-39-8 1-[(4R,6R)-(2,2-dimethyl-6-tridecyl-[1,3]dioxan-4-yl)]-4-(4-hydroxyphenyl)-butan-2-one 
• 913814-38-7 (3R,7R)-3-Benzyloxy-1-(4-benzyloxy-phenyl)-7-hydroxy-icosan-5-one 
• 871809-96-0 (3R,5R,7R)-3-benzyloxy-1-(4-benzyloxyphenyl)eicosane-5,7-diol 

Relevant articles and documents

Enantioselective synthesis and absolute configurations of aculeatins A, B, D, and 6-epi-aculeatin D

The three naturally occurring, bioactive spiroacetals aculeatins A, B, and D, as well as the non-natural 6-epi-aculeatin D have been synthesized for the first time in enantiopure form using an asymmetric allylation as the only chirality source. A further

Enantioselective synthesis and absolute configurations of aculeatins A and B

The two naturally occuring, bioactive spiroacetals aculeatins A and B have been synthesized for the first time in enantiopure form using an asymmetric allylation as the only chirality source. A further key step was a stereoselective aldol reaction with re