160796-76-9

Basic information

• Product Name: (2R,3S,4R,5S,6S,9R,10R,11R,12R,13R)-3,5-<(p-bromobenzylidene)dioxy>-9,11-dihydroxy-2,4,6,10,12,13-hexamethyl-8-methylenetetradecanolide
• Synonyms: (2R,3S,4R,5S,6S,9R,10R,11R,12R,13R)-3,5-<(p-bromobenzylidene)dioxy>-9,11-dihydroxy-2,4,6,10,12,13-hexamethyl-8-methylenetetradecanolide
• CAS NO: 160796-76-9
• Molecular Weight: 539.507
• Mol File: 160796-76-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3S,4R,5S,6S,9R,10R,11R,12R,13R)-3,5-<(p-bromobenzylidene)dioxy>-9,11-dihydroxy-2,4,6,10,12,13-hexamethyl-8-methylenetetradecanolide(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S,4R,5S,6S,9R,10R,11R,12R,13R)-3,5-<(p-bromobenzylidene)dioxy>-9,11-dihydroxy-2,4,6,10,12,13-hexamethyl-8-methylenetetradecanolide(160796-76-9)
• EPA Substance Registry System: (2R,3S,4R,5S,6S,9R,10R,11R,12R,13R)-3,5-<(p-bromobenzylidene)dioxy>-9,11-dihydroxy-2,4,6,10,12,13-hexamethyl-8-methylenetetradecanolide(160796-76-9)

Safety Data

• Hazardous Substances Data: 160796-76-9(Hazardous Substances Data)

Upstream product

• 24856-58-4 1,1-dimethoxy-1-(4-bromophenyl)methane 
• 119870-68-7 (2R,3S,4R,5S,6S,9R,10R,11R,12R,13R)-3,5,9,11-tetrahydroxy-2,4,6,10,12,13-hexamethyl-8-methylenetetradecanolide 

Downstream Products

• 156766-85-7 (2R,3S,4R,5S,6S,8S,10R,11R,12R,13R)-3,5-<(p-bromobenzylidene)dioxy>-8,8-(epoxymethano)-11-hydroxy-2,4,6,10,12,13-hexamethyl-9-oxotetradecanolide 
• 156766-84-6 (2R,3S,4R,5S,6S,8S,9R,10R,11R,12R,13R)-3,5-<(p-bromobenzylidene)dioxy>-8,8-(epoxymethano)-9,11-dihydroxy-2,4,6,10,12,13-hexamethyltetradecanolide 

Relevant articles and documents

Studies in macrolide synthesis: A stereocontrolled synthesis of oleandolide employing reagent- and substrate-controlled aldol reactions of (S)-1-(benzyloxy)-2-methylpentan-3-one

A highly stereocontrolled total synthesis of oleandolide (2), the aglycon of the macrolide antibiotic oleandomycin (1), has been completed in 8% overall yield (20 steps longest linear sequence, 26 steps in total) with 90% overall diastereoselectivity. Ini