15330-39-9

Basic information

• Product Name: 7a,14c-dihydronaphtho<2,1-b>naphtho<2',1':5,6>furo<3,2-d>furan
• Synonyms: 7a,14c-dihydronaphtho<2,1-b>naphtho<2',1':5,6>furo<3,2-d>furan
• CAS NO: 15330-39-9
• Molecular Weight: 310.352
• Mol File: 15330-39-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7a,14c-dihydronaphtho<2,1-b>naphtho<2',1':5,6>furo<3,2-d>furan(CAS DataBase Reference)
• NIST Chemistry Reference: 7a,14c-dihydronaphtho<2,1-b>naphtho<2',1':5,6>furo<3,2-d>furan(15330-39-9)
• EPA Substance Registry System: 7a,14c-dihydronaphtho<2,1-b>naphtho<2',1':5,6>furo<3,2-d>furan(15330-39-9)

Safety Data

• Hazardous Substances Data: 15330-39-9(Hazardous Substances Data)

Upstream product

• 131543-46-9 Glyoxal 
• 36294-21-0 potassium 2-naphthoxide 

Downstream Products

• 60964-81-0 2,2'-diacetoxy-1,1'-dinaphthylmethane 
• 1096-84-0 bis(2-hydroxy-1-naphthyl)methane 

Relevant articles and documents

Base-Catalyzed Alkylation of 2-Naphthol with Glyoxal

Alkylation of potassium 2-naphthyl oxide with glyoxal in aqueous media formed 1,2-dihydronaphthofuran-1,2-diol (1).Without isolation of 1, acidification of this reaction mixture with aqueous HCl led to three products, i.e., the lactone of (2-hydroxy-1-naphthyl)acetic acid (2), the hemiacetal of bis(2-hydroxy-1-naphthyl)acetaldehyde (3), and the corresponding acetal (4).Mutual interconversions of 1 and these three products revealed the reaction pathway and the mechanisms of formation of the lactone and the acetal.