727723-14-0

Basic information

• Product Name: 1-(2,6-Dimethoxy-phenyl)-2-((4aR,6aS,7R,10aS,10bR)-3,3,6a,10b-tetramethyl-8-methylene-decahydro-naphtho[2,1-d][1,3]dioxin-7-yl)-ethanol
• Synonyms: 1-(2,6-Dimethoxy-phenyl)-2-((4aR,6aS,7R,10aS,10bR)-3,3,6a,10b-tetramethyl-8-methylene-decahydro-naphtho[2,1-d][1,3]dioxin-7-yl)-ethanol
• CAS NO: 727723-14-0
• Molecular Weight: 444.612
• Mol File: 727723-14-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(2,6-Dimethoxy-phenyl)-2-((4aR,6aS,7R,10aS,10bR)-3,3,6a,10b-tetramethyl-8-methylene-decahydro-naphtho[2,1-d][1,3]dioxin-7-yl)-ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,6-Dimethoxy-phenyl)-2-((4aR,6aS,7R,10aS,10bR)-3,3,6a,10b-tetramethyl-8-methylene-decahydro-naphtho[2,1-d][1,3]dioxin-7-yl)-ethanol(727723-14-0)
• EPA Substance Registry System: 1-(2,6-Dimethoxy-phenyl)-2-((4aR,6aS,7R,10aS,10bR)-3,3,6a,10b-tetramethyl-8-methylene-decahydro-naphtho[2,1-d][1,3]dioxin-7-yl)-ethanol(727723-14-0)

Safety Data

• Hazardous Substances Data: 727723-14-0(Hazardous Substances Data)

Upstream product

• 372939-36-1 (S,E)-5-oxo-4-(2-((4aR,6aS,7R,10aS, 10bR)-3,3,6a,10b-tetramethyl-8-methylenedecahydro-1H-naphtho[2,1-d][1,3]dioxin-7-yl)ethylidene)tetrahydrofuran-3-yl acetate 
• 372939-35-0 3,18-O-isopropylideneandrographolide 
• 727723-05-9 (E)-3-(2-((4aR,6aS,7R,10bR)-3,3,6a,10b-tetramethyl-8-methylenedecahydro-1H-naphtho[2,1-d][1,3]dioxin-7-yl)ethylidene)furan-2(3H)-one 
• 142037-79-4 andrographolide 
• 151-10-0 1,3-Dimethoxybenzene 
• 727723-06-0 2-((4aR,6aS,7R,10aS,10bR)-3,3,6a,10b-tetramethyl-8-methylenedecahydro-1H-naphtho[2,1-d][1,3]dioxin-7-yl)acetaldehyde 

Relevant articles and documents

Novel routes for the generation of structurally diverse labdane diterpenes from andrographolide

Andrographolide 1, the major constituent of the Indian medicinal plant Andrographis paniculata (Acanthaceae) was converted into the key intermediate 4 by selective oxidative degradation of the C-12,13 olefin bond. The aldehyde functional group present in 4 has been utilized for synthesizing a number of structurally diverse labdane diterpenes. Synthesis and in vitro cytotoxic activity results of the compounds prepared are discussed.