23676-21-3

Basic information

• Product Name: 2-Naphthalenol, 1-(3-methyl-2-butenyl)-
• CAS NO: 23676-21-3
• Molecular Formula: C15H16O
• Molecular Weight: 212.291
• Mol File: 23676-21-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Naphthalenol, 1-(3-methyl-2-butenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Naphthalenol, 1-(3-methyl-2-butenyl)-(23676-21-3)
• EPA Substance Registry System: 2-Naphthalenol, 1-(3-methyl-2-butenyl)-(23676-21-3)

Safety Data

• Hazardous Substances Data: 23676-21-3(Hazardous Substances Data)

Upstream product

• 574-00-5 1,2-Dihydroxynaphthalene 
• 870-63-3 prenyl bromide 
• 135-19-3 β-naphthol 
• 598-25-4 Dimethylallene 

Downstream Products

• 19836-62-5 3,3-dimethyl-3H-benzo[f]chromene 
• 1269598-89-1 C₃₁H₃₄OSi 

Relevant articles and documents

REGIOSPECIFIC CATALYTIC ALKENYLATION OF AROMATIC SUBSTRATES WITH COORDINATED DIENES: REACTIONS ON NAPHTHALENE DERIVATIVES. PRELIMINARY RESULTS ON HETEROAROMATIC SUBSTRATES

α- and β-naphthol undergo regiospecific alkenylation by 1,1-dimethylallene (DMA) at the OH-adjacent β- and α-positions, respectively, when allowed to react with DMA-Pt(II) complex.A catalytic process can be achieved with conversions higher than 90percent.A Pd(II) complex as promotor and isoprene as alkenylating diene can also be used.Similar results were obtained with N-acetyl-β-naphthylamine.Preliminary results indicated that nitrogen-containing heteroaromatic substrates can afford N-, O- or C-isopentenyl derivatives depending on the particular features of the organic ring.