96965-64-9

Basic information

• Product Name: 3,6-dibromo-2,7-bis<(p-tolylsulfonyl)oxy>naphthalene
• Synonyms: 3,6-dibromo-2,7-bis<(p-tolylsulfonyl)oxy>naphthalene
• CAS NO: 96965-64-9
• Molecular Weight: 626.343
• Mol File: 96965-64-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,6-dibromo-2,7-bis<(p-tolylsulfonyl)oxy>naphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-dibromo-2,7-bis<(p-tolylsulfonyl)oxy>naphthalene(96965-64-9)
• EPA Substance Registry System: 3,6-dibromo-2,7-bis<(p-tolylsulfonyl)oxy>naphthalene(96965-64-9)

Safety Data

• Hazardous Substances Data: 96965-64-9(Hazardous Substances Data)

Upstream product

• 96965-79-6 2,7-dibromo-3,6-dihydroxy naphthalene 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 92-24-0 Tetracen 

Relevant articles and documents

Twin Benzoannulation of Naphthalene via 1,3-, 1,6-, and 2,6-Naphthodiyne Synthetic Equivalents. New Syntheses of Triphenylene, Benzanthracene, and Naphthacene

New syntheses of triphenylene (4), benzanthracene (5), naphthacene (6), and the tetramethylated derivatives 17 and 25 are described that feature, as the key step, the formal Diels-Alder cycloaddition between a naphthodiyne synthon (1, 2, or 3) and a furan (10 or 14).Subsequent deoxygenation affords the arene in 16-28percent overall yield from dibromo ditosylate 7, 8, or 9.The latter are prepared in two steps from commercially available 2,3- or 2,7-dihydroxynaphthalene, and, with phenyllithium, serve as synthetic equivalents of 1, 2, and 3.The X-ray structure of the anti isomer of 23 is discussed in some detail.