426820-51-1

Basic information

• Product Name: 2,4-bis-benzyloxy-5-bromo-phenol
• Synonyms: 2,4-bis-benzyloxy-5-bromo-phenol
• CAS NO: 426820-51-1
• Molecular Weight: 385.257
• Mol File: 426820-51-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,4-bis-benzyloxy-5-bromo-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-bis-benzyloxy-5-bromo-phenol(426820-51-1)
• EPA Substance Registry System: 2,4-bis-benzyloxy-5-bromo-phenol(426820-51-1)

Safety Data

• Hazardous Substances Data: 426820-51-1(Hazardous Substances Data)

Upstream product

• 6195-80-8 2,4-bis(benzyloxy)phenol 
• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 100-39-0 benzyl bromide 
• 13246-46-3 2,4-dibenzyloxybenzaldehyde 

Downstream Products

• 622390-73-2 [4,6-dihydroxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenyl]-(2,4-dihydroxy-5-methoxy-phenyl)-methanone 
• 622390-85-6 [4,6-bis-benzyloxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenyl]-(2,4-bis-benzyloxy-5-methoxy-phenyl)-methanone 
• 622390-71-0 [4,6-bis-benzyloxy-2-methoxymethoxy-3-(3-methyl-but-2-enyl)-phenyl]-(2,4-bis-benzyloxy-5-methoxy-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 
• 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 
• 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 
• 426820-41-9 1,5-Bis-benzyloxy-2-bromo-4-methoxy-3-(3-methyl-but-2-enyl)-benzene 
• 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 
• 426820-52-2 (3,5-bis-benzyloxy-2-bromo-6-methoxy-phenyl)-acetaldehyde 
• 6147-11-1 α-mangostin 
• 622390-57-2 1,5-Bis-benzyloxy-2-bromo-4-methoxy-benzene 
• 426820-39-5 1-Allyloxy-2,4-bis-benzyloxy-5-bromo-benzene 

Relevant articles and documents

Biological activities of α-mangostin derivatives against acidic sphingomyelinase

Deprenyl and benzofenone-type congeners of α-mangostin 1 have been synthesized to understand their role for the inhibitory activity against sphingomyelinase (SMase). While removal of the prenyl group of the right side (11 and 12) caused loss of the selectivity between ASMase (acidic sphingomyelinase) and NSMase (neutral sphingomyelinase), the prenyl group of the left side appeared to increase the inhibitory activities (16 and 17).