603964-55-2

Basic information

• Product Name: 6-((2R,4R,5R,6R)-4,5-Bis-benzyloxy-6-methyl-tetrahydro-pyran-2-yl)-2-bromo-5-methoxy-[1,4]naphthoquinone
• Synonyms: 6-((2R,4R,5R,6R)-4,5-Bis-benzyloxy-6-methyl-tetrahydro-pyran-2-yl)-2-bromo-5-methoxy-[1,4]naphthoquinone
• CAS NO: 603964-55-2
• Molecular Weight: 577.472
• Mol File: 603964-55-2.mol

Chemical Properties

• CAS DataBase Reference: 6-((2R,4R,5R,6R)-4,5-Bis-benzyloxy-6-methyl-tetrahydro-pyran-2-yl)-2-bromo-5-methoxy-[1,4]naphthoquinone(CAS DataBase Reference)
• NIST Chemistry Reference: 6-((2R,4R,5R,6R)-4,5-Bis-benzyloxy-6-methyl-tetrahydro-pyran-2-yl)-2-bromo-5-methoxy-[1,4]naphthoquinone(603964-55-2)
• EPA Substance Registry System: 6-((2R,4R,5R,6R)-4,5-Bis-benzyloxy-6-methyl-tetrahydro-pyran-2-yl)-2-bromo-5-methoxy-[1,4]naphthoquinone(603964-55-2)

Safety Data

• Hazardous Substances Data: 603964-55-2(Hazardous Substances Data)

Upstream product

• 551939-59-4 2-((2R,4R,5R,6R)-4,5-bis(benzyloxy)-6-methyltetrahydro-2H-pyran-2-yl)-5,8-dimethoxynaphthalen-1-ol 
• 171081-04-2 6-(3,4-di-O-benzyl-2,6-dideoxy-β-D-arabino-hexopyranosyl)-5-methoxy-1,4-naphthoquinone 

Relevant articles and documents

General entries to C-aryl glycosides. Formal synthesis of galtamycinone

Utilizing a general entry we had developed for the synthesis of C-aryl glycosides, we have prepared the juglone derivatives 18-20 as well as the juglone precursor 13. Because 19 had been previously converted in two steps by Suzuki into galtamycinone (1), its preparation constitutes a total synthesis of 1.