1628535-39-6

Basic information

• Product Name: 5-(bromomethyl)-7-methoxy-2,2-dimethyl-4H-benzo[d][1,3]-dioxin-4-one
• Synonyms: 5-(bromomethyl)-7-methoxy-2,2-dimethyl-4H-benzo[d][1,3]-dioxin-4-one
• CAS NO: 1628535-39-6
• Molecular Weight: 301.137
• Mol File: 1628535-39-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-(bromomethyl)-7-methoxy-2,2-dimethyl-4H-benzo[d][1,3]-dioxin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(bromomethyl)-7-methoxy-2,2-dimethyl-4H-benzo[d][1,3]-dioxin-4-one(1628535-39-6)
• EPA Substance Registry System: 5-(bromomethyl)-7-methoxy-2,2-dimethyl-4H-benzo[d][1,3]-dioxin-4-one(1628535-39-6)

Safety Data

• Hazardous Substances Data: 1628535-39-6(Hazardous Substances Data)

Upstream product

• 2524-37-0 ethyl orselinate 

Downstream Products

• 66018-41-5 zeaenol 
• 1628535-34-1 7-methoxy-2,2-dimethyl-5-((1-phenyl-1H-tetrazol-5-ylsulfon-yl)-methyl)-4H-benzo[d][1,3]dioxin-4-one 
• 1628535-40-9 7-methoxy-2,2-dimethyl-5-((1-phenyl-1H-tetrazol-5-ylthio)-methyl)-4H-benzo[d][1,3]dioxin-4-one 

Relevant articles and documents

Stereoselective synthesis of resorcylic acid lactone Cochliomycin B

The total synthesis of 14-membered resorcylic acid lactone, Cochliomycin B has prescribed, in a convergent manner, from readily available starting materials, D-galactose, L-aspartic acid and ethyl acetoacetate. The key reactions involved in the synthesis are Julia-Kocienski olefination, E-selective Horner-Wadsworth-Emmons olefination and intramolecular lactonization.