709640-13-1

Basic information

• Product Name: 3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenyl ethanoate
• Synonyms: 3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenyl ethanoate
• CAS NO: 709640-13-1
• Molecular Weight: 544.515
• Mol File: 709640-13-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenyl ethanoate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenyl ethanoate(709640-13-1)
• EPA Substance Registry System: 3-acetyl-3,5,12-trihydroxy-6,11-dioxo-1,2,3,4,6,11-hexahydro-1-naphthacenyl 2-(acetyloxy)-2-phenyl ethanoate(709640-13-1)

Safety Data

• Hazardous Substances Data: 709640-13-1(Hazardous Substances Data)

Upstream product

• 7322-88-5 (S)-acetylmandelic acid 
• 60660-75-5 (+/-)-9-acetyl-6,7,9,11-tetrahydroxy-7,8,9,10-tetrahydronaphthacen-5,12-dione 
• 67122-26-3 2-acetyl-1,2,3,4,6,11-hexahydro-5,12-dihydroxynaphthacene-6,11-quinone 
• 84700-18-5 6,7,9,11-tetrahydroxy-9-(2-methyl-[1,3]dioxolan-2-yl)-7,8,9,10-tetrahydro-naphthacene-5,12-dione 
• 86423-66-7 6,8,11-trihydroxy-8-(2-methyl-[1,3]dioxolan-2-yl)-7,8,9,10-tetrahydro-naphthacene-5,12-dione 
• 150-78-7 1,4-dimethoxybezene 
• 41098-99-1 1,2,3,4-tetrahydro-5,8-dimethoxy-4-oxonaphthalene-2-carboxylic acid 
• 33628-85-2 (+/-)-2-acetyl-2-hydroxy-1,2,3,4-tetrahydro-5,8-dimethoxynaphthalene 
• 65529-77-3 4-demethoxy-7-deoxydaunomycinone 
• 33654-68-1 1-(5,8-dimethoxy-1,2,3,4-tetrahydro-2-naphthalenyl)-1-ethanone 

Relevant articles and documents

Facile total syntheses of idarubicinone-7-β-D-glucuronide: Convenient preparations of AB-ring synthon using some carboxylic acid derivatives

Regiospecific syntheses of idarubicinone coupled with D-glucuronic acid are described. Cyclization of dimethoxybenzene with carboxylic acid derivatives in polyphosphoric acid (PPA) in one step afforded the naphthalenones 7, which were transformed to the (