426820-41-9

Basic information

• Product Name: 1,5-Bis-benzyloxy-2-bromo-4-methoxy-3-(3-methyl-but-2-enyl)-benzene
• Synonyms: 1,5-Bis-benzyloxy-2-bromo-4-methoxy-3-(3-methyl-but-2-enyl)-benzene
• CAS NO: 426820-41-9
• Molecular Weight: 467.403
• Mol File: 426820-41-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,5-Bis-benzyloxy-2-bromo-4-methoxy-3-(3-methyl-but-2-enyl)-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-Bis-benzyloxy-2-bromo-4-methoxy-3-(3-methyl-but-2-enyl)-benzene(426820-41-9)
• EPA Substance Registry System: 1,5-Bis-benzyloxy-2-bromo-4-methoxy-3-(3-methyl-but-2-enyl)-benzene(426820-41-9)

Safety Data

• Hazardous Substances Data: 426820-41-9(Hazardous Substances Data)

Upstream product

• 24470-78-8 isopropyltriphenylphosphonium iodide 
• 426820-52-2 (3,5-bis-benzyloxy-2-bromo-6-methoxy-phenyl)-acetaldehyde 
• 426820-40-8 3-Allyl-1,5-bis-benzyloxy-2-bromo-4-methoxy-benzene 
• 426820-56-6 2-allyl-4,6-bis-benzyloxy-3-bromo-phenol 
• 426820-39-5 1-Allyloxy-2,4-bis-benzyloxy-5-bromo-benzene 
• 426820-51-1 2,4-bis-benzyloxy-5-bromo-phenol 
• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 100-39-0 benzyl bromide 
• 6195-80-8 2,4-bis(benzyloxy)phenol 

Downstream Products

• 6147-11-1 α-mangostin 
• 426820-49-7 [4,6-dihydroxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenyl]-[4,6-dihydroxy-3-methoxy-2-(3-methyl-but-2-enyl)-phenyl]-methanone 
• 426820-55-5 [4,6-bis-benzyloxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenyl]-[4,6-bis-benzyloxy-3-methoxy-2-(3-methyl-but-2-enyl)-phenyl]-methanone 
• 622390-63-0 [4,6-bis-benzyloxy-3-methoxy-2-(3-methyl-but-2-enyl)-phenyl]-(2,4,6-tris-methoxymethoxy-phenyl)-methanol 
• 426820-48-6 [4,6-bis-benzyloxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenyl]-[4,6-bis-benzyloxy-3-methoxy-2-(3-methyl-but-2-enyl)-phenyl]-methanol 

Relevant articles and documents

The first direct synthesis of α-mangostin, a potent inhibitor of the acidic sphingomyelinase

A total synthesis of α-mangostin 1a has been achieved. The key cyclization reaction to construct the xanthone framework was undertaken by employing the PPh3-CCl4 conditions. The inhibitory activities of 1a and the benzophenone intermediate 16 against the acidic sphingomyelinase were discussed.