111492-49-0

Basic information

• Product Name: 1-<6'-benzyloxy-3',4'-dimethoxy-2-(prop-1-enyl)phenyl>-4-(2-methyl-1,3-dioxolan-2-yl)-2-methylenebutane-1,3-dione
• Synonyms: 1-<6'-benzyloxy-3',4'-dimethoxy-2-(prop-1-enyl)phenyl>-4-(2-methyl-1,3-dioxolan-2-yl)-2-methylenebutane-1,3-dione
• CAS NO: 111492-49-0
• Molecular Weight: 466.531
• Mol File: 111492-49-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-<6'-benzyloxy-3',4'-dimethoxy-2-(prop-1-enyl)phenyl>-4-(2-methyl-1,3-dioxolan-2-yl)-2-methylenebutane-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-<6'-benzyloxy-3',4'-dimethoxy-2-(prop-1-enyl)phenyl>-4-(2-methyl-1,3-dioxolan-2-yl)-2-methylenebutane-1,3-dione(111492-49-0)
• EPA Substance Registry System: 1-<6'-benzyloxy-3',4'-dimethoxy-2-(prop-1-enyl)phenyl>-4-(2-methyl-1,3-dioxolan-2-yl)-2-methylenebutane-1,3-dione(111492-49-0)

Safety Data

• Hazardous Substances Data: 111492-49-0(Hazardous Substances Data)

Upstream product

• 95730-76-0 1-<6'-benzyloxy-3',4'-dimethoxy-2'-(prop-1-enyl)phenyl>-4-(2-methyl-1,3-dioxolan-2-yl)-2-(methylthiomethyl)butane-1,3-dione 
• 95730-74-8 6'benzyloxy-3-hydroxy-3',4'-dimethoxy-4-(2-methyl-1,3-dioxolan-2-yl)-2'-(prop-1-enyl)butyrophenone 
• 125288-40-6 1-<6'-benzyloxy-3',4'-dimethoxy-2'-(prop-1-enyl)phenyl>-4-(2-methyl-1,3-dioxolan-2-yl)butane-1,3-dione 
• 95730-73-7 6-benzyloxy-3,4-dimethoxy-2-(prop-1-enyl)acetophenone 
• 18871-63-1 3,3-ethylenedioxybutanal 
• 95730-77-1 1-<6'-benzyloxy-3',4'-dimethoxy-2-(prop-1-enyl)phenyl>-4-(2-methyl-1,3-dioxolan-2-yl)-2-(methylsulphinylmethyl)butane-1,3-dione 

Downstream Products

• 479-66-3 (-)-neurochromenin 

Relevant articles and documents

Studies on the Syntheses of Heterocyclic Compounds containing Benzopyrone. Part 5. Total Synthesis of Fulvic Acid

Total synthesis of fulvic acid (1a) is described.Regioselective cyclization of the enedione (8f), an equivalent of the proposed biogenetic intermediate (5a) for citromycetin (2), gave the pyrone (11a), which led to fulvic acid (1a) by a route involving debenzylation, selective ozonization, and hydration.