4816-00-6

Basic information

• Product Name: Benzaldehyde, 2-bromo-4,5-bis(phenylmethoxy)-
• CAS NO: 4816-00-6
• Molecular Formula: C21H17BrO3
• Molecular Weight: 397.268
• Mol File: 4816-00-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 2-bromo-4,5-bis(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 2-bromo-4,5-bis(phenylmethoxy)-(4816-00-6)
• EPA Substance Registry System: Benzaldehyde, 2-bromo-4,5-bis(phenylmethoxy)-(4816-00-6)

Safety Data

• Hazardous Substances Data: 4816-00-6(Hazardous Substances Data)

Upstream product

• 4815-99-0 2-bromo-4,5-dihydroxybenzoaldehyde 
• 100-39-0 benzyl bromide 
• 2973-59-3 2-bromoisovanillin 
• 79822-80-3 3-(chloromethoxy)-4-hydroxy-6-bromobenzaldehyde 
• 15930-53-7 6-bromo-3,4-methylenedioxybenzaldehyde 
• 5447-02-9 3,4-dibenzyloxybenzaldehyde 
• 100-44-7 benzyl chloride 

Downstream Products

• 1030376-89-6 alterlactone 
• 1170034-89-5 7,7'-Dimethoxy-2,2,2',2'-tetramethyl-4,4'-dioxo-4H,4'H-[5,5']-bi(benzo[d][1,3]dioxinyl) 
• 1371598-34-3 9,10-bis(benzyloxy)-4-hydroxy-2-methoxy-dibenzo[c,e]oxepin-5(7H)-one 
• 31186-12-6 altenusin 
• 79822-78-9 6-(1-acetoxyprop-2-enyl)-3,4-bis(benzyloxy)-1-(1,3-dioxolan-2-yl)benzene 
• 79822-69-8 3,4-bis(benzyloxy)-1-(1,3-dioxolan-2-yl)-6-(1-hydroxyprop-2-enyl)benzene 
• 344581-69-7 4,5-bis(benzyloxy)-6-(3-chloroprop-1-enyl)-1-(1,3-dioxolan-2-yl)benzene 
• 344586-57-8 1-[4,5-Bis-benzyloxy-2-((E)-propenyl)-phenyl]-2-isopropylamino-ethanol 
• 344592-79-6 3,4-bis(benzyloxy)-6-(prop-1-enyl)benzaldehyde 
• 344572-49-2 2-[4,5-Bis-benzyloxy-2-((E)-propenyl)-phenyl]-oxirane 
• 120566-83-8 N-<3,4-dimethoxyphenethyl>-4',5'-dibenzyloxy-2'-bromophenylacetamide 
• 120566-85-0 1-<2'-bromo-4',5'-dibenzyloxybenzyl>-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 
• 120566-81-6 2-bromo-4,5-dibenzyloxyphenylacetic acid 
• 120566-82-7 2-bromo-4,5-dibenzyloxyphenylacetyl chloride 

Relevant articles and documents

Total synthesis of altenusin and alterlactone

The resorcylic lactone alterlactone, a mycotoxin produced by alternaria sp., was synthesized for the first time. The total synthesis was achieved in nine steps with 69% yield starting with acetal-protected phloroglucinic acid and 6-bromopiperonal, where t

Studies on Mannich Reaction of 1-Benzyltetrahydroisoquinolines

The effect of substituents in Mannich cyclisation reaction of 1-benzyltetrahydroisoquinolines has been studied.Both para- and ortho-cyclisation products are formed when hydroxyl groups are present in the benzene ring of the benzylic moiety whereas only pa