1452153-45-5

Basic information

• Product Name: methyl 5-hydroxy-2-methyl-2-phenyl-2,3-dihydronaphtho[1,2-b]furan-4-carboxylate
• Synonyms: methyl 5-hydroxy-2-methyl-2-phenyl-2,3-dihydronaphtho[1,2-b]furan-4-carboxylate
• CAS NO: 1452153-45-5
• Molecular Weight: 334.372
• Mol File: 1452153-45-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 5-hydroxy-2-methyl-2-phenyl-2,3-dihydronaphtho[1,2-b]furan-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 5-hydroxy-2-methyl-2-phenyl-2,3-dihydronaphtho[1,2-b]furan-4-carboxylate(1452153-45-5)
• EPA Substance Registry System: methyl 5-hydroxy-2-methyl-2-phenyl-2,3-dihydronaphtho[1,2-b]furan-4-carboxylate(1452153-45-5)

Safety Data

• Hazardous Substances Data: 1452153-45-5(Hazardous Substances Data)

Upstream product

• 77060-74-3 methyl 1,4-dihydroxy-2-naphthoate 
• 31519-22-9 1,4-dihydroxy-2-naphthoic acid 
• 83575-14-8 2-methoxycarbonyl-1,4-naphthoquinone 
• 98-83-9 isopropenylbenzene 

Relevant articles and documents

Dihydronaphtho[1,2-b]furan derivatives and synthesis method thereof

The present invention relates to dihydronaphtho[1,2-b]furan derivatives and a synthesis method thereof, wherein different kinds of dihydronaphtho[1,2-b]furan derivatives representing various biological activities can be synthesized through a one-pot process with high yield. In addition, the synthesized dihydronaphtho[1,2-b]furan can be easily synthesized using a key step to furumollugin in a second step.COPYRIGHT KIPO 2015

A novel and efficient synthesis of diverse dihydronaphtho[1,2-b]furans using the ceric ammonium nitrate-catalyzed formal [3 + 2] cycloaddition of 1,4-naphthoquinones to olefins and its application to furomollugin

A novel approach was developed for the synthesis of diverse dihydronaphtho[1,2-b]furans from 1,4-naphthoquinones and olefins in the presence of ceric ammonium nitrate. This reaction provides a rapid route for the synthesis of a variety of dihydronaphtho[1,2-b]furans and naphtho[1,2-b]furans bearing different substituents. This methodology was also used to synthesize the biologically important natural product furomollugin in only 2 steps. The Royal Society of Chemistry.