362662-60-0

Basic information

• Product Name: 4-benzyloxy-3-bromo-5-methoxy-phenol
• Synonyms: 4-benzyloxy-3-bromo-5-methoxy-phenol
• CAS NO: 362662-60-0
• Molecular Weight: 309.159
• Mol File: 362662-60-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-benzyloxy-3-bromo-5-methoxy-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-benzyloxy-3-bromo-5-methoxy-phenol(362662-60-0)
• EPA Substance Registry System: 4-benzyloxy-3-bromo-5-methoxy-phenol(362662-60-0)

Safety Data

• Hazardous Substances Data: 362662-60-0(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 2973-76-4 5-bromo-4-hydroxy-3-methoxybenzaldehyde 
• 2556-04-9 4-(benzyloxy)-3-bromo-5-methoxybenzaldehyde 
• 121-33-5 vanillin 

Downstream Products

• 62385-85-7 2,5,8-trimethoxynaphthalene-1,4-dione 
• 64421-39-2 anhydrofusarubin 
• 905811-38-3 1-benzyloxy-2,4,5,8-tetramethoxynaphthalene 
• 905811-36-1 1,2-dibromo-3-benzyloxy-4,6-dimethoxybenzene 
• 61654-68-0 2,5-bis-benzyloxy-1-bromo-3-methoxy-benzene 

Relevant articles and documents

Unified synthesis and cytotoxic activity of 8-O -methylfusarubin and its analogues

A simple and unified synthesis of four related pyranonaphthoquinone natural products, e.g. 8-O-methylfusarubin, 8-O-methylanhydrofusarubin, fusarubin and anhydrofusarubin, is reported. The key synthetic features include the precedented Diels-Alder cycload

Synthesis of the naphthalene portion of the rubromycins.

[reaction: see text]. A synthesis of a reduced version of the naphthazarin found in the rubromycin class of natural products is reported. The naphthalene ring system is formed via a Doetz reaction with a symmetrical alkyne. Differentiation between the C1'