1315340-92-1

Basic information

• Product Name: 5-(2-benzyloxy-phenyl)-3-(1,4,5,6,8-pentamethoxynaphthalen-2-ylmethyl)-4,5-dihydro-isoxazole
• Synonyms: 5-(2-benzyloxy-phenyl)-3-(1,4,5,6,8-pentamethoxynaphthalen-2-ylmethyl)-4,5-dihydro-isoxazole
• CAS NO: 1315340-92-1
• Molecular Weight: 543.617
• Mol File: 1315340-92-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-(2-benzyloxy-phenyl)-3-(1,4,5,6,8-pentamethoxynaphthalen-2-ylmethyl)-4,5-dihydro-isoxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(2-benzyloxy-phenyl)-3-(1,4,5,6,8-pentamethoxynaphthalen-2-ylmethyl)-4,5-dihydro-isoxazole(1315340-92-1)
• EPA Substance Registry System: 5-(2-benzyloxy-phenyl)-3-(1,4,5,6,8-pentamethoxynaphthalen-2-ylmethyl)-4,5-dihydro-isoxazole(1315340-92-1)

Safety Data

• Hazardous Substances Data: 1315340-92-1(Hazardous Substances Data)

Upstream product

• 114263-49-9 1,4,5,6,8-pentamethoxynaphthalene-2-carbaldehyde 
• 122182-21-2 1,2,4,5,8-pentamethoxynaphthalene 
• 1315340-90-9 1,2,4,5,8-pentamethoxy-6-(2-nitro-ethyl)-naphthalene 
• 67191-36-0 1-(benzyloxy)-2-ethenylbenzene 

Downstream Products

• 1315340-94-3 4-(2-benzyloxy-phenyl)-4-(tert-butyldimethylsilanyloxy)-1-(1,4,5,6,8-pentamethoxy-naphthalen-2-yl)-butan-2-one 
• 1315340-93-2 4-(2-benzyloxy-phenyl)-4-hydroxy-1-(1,4,5,6,8-pentamethoxy-naphthalen-2-yl)-butan-2-one 
• 1315340-95-4 6-[4-(2-benzyloxy-phenyl)-4-(tert-butyldimethylsilanyloxy)-2-oxo-butyl]-2,5,8-trimethoxy-[1,4]naphthoquinone 
• 1315340-96-5 2-[4-(2-benzyloxy-phenyl)-4-(tert-butyldimethylsilanyloxy)-2-oxo-butyl]-5,6,8-trimethoxy-[1,4]naphthoquinone 
• 1315340-99-8 C₂₃H₂₂O₇ 
• 1315340-97-6 6-[4-(tert-butyldimethylsilanyloxy)-4-(2-hydroxy-phenyl)-2-oxo-butyl]-2,5,8-trimethoxy-[1,4]naphthoquinone 
• 1315340-98-7 6-[4-(tert-butyldimethylsilanyloxy)-4-(2-hydroxy-phenyl)-2-oxo-butyryl]-2,5,8-trimethoxy-[1,4]naphthoquinone 

Relevant articles and documents

Alternative spiroketalization methods toward purpuromycin: A hemiketal conjugate addition strategy and use of an electron-rich isocoumarin precursor

Two methods are presented that were designed to circumvent the persistent problem of benzofuran formation and instead yield a spiroketal of the rubromycin family type. First, using an alternative disconnection, a hemiketal conjugate addition to a naphthaq