111436-61-4

Basic information

• Product Name: Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy-
• CAS NO: 111436-61-4
• Molecular Formula: C15H13BrO3
• Molecular Weight: 321.17
• Mol File: 111436-61-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy-(111436-61-4)
• EPA Substance Registry System: Benzaldehyde, 3-[4-(bromomethyl)phenoxy]-4-methoxy-(111436-61-4)

Safety Data

• Hazardous Substances Data: 111436-61-4(Hazardous Substances Data)

Upstream product

• 111436-60-3 methyl 4-<2-methoxy-5-(1,3-dioxan-2-yl)phenoxy>benzoate 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 208399-65-9 4-(5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy)benzaldehyde 
• 459-57-4 4-fluorobenzaldehyde 
• 621-59-0 isovanillin 
• 181758-85-0 2-(3-hydroxy-4-methoxyphenyl)-1,3-dioxolane 
• 208399-64-8 {4-[5-(1,3-dioxolan-2-yl)-2-methoxyphenoxy]phenyl}methanol 
• 101553-98-4 {4-[5-(1,3-dioxan-2-yl)-2-methoxyphenoxy]phenyl}methanol 
• 101110-74-1 methyl 4-(5'-formyl-2'-methoxyphenoxy)benzoate 

Downstream Products

• 111436-64-7 3-(4-{2-[3-(4-Hydroxymethyl-2-methoxy-phenoxy)-phenyl]-ethyl}-phenoxy)-4-methoxy-benzaldehyde 
• 101613-53-0 4-(3-{(E)-2-[4-(5-[1,3]Dioxan-2-yl-2-methoxy-phenoxy)-phenyl]-vinyl}-phenoxy)-3-methoxy-benzoic acid methyl ester 
• 111436-63-6 4-(3-{2-[4-(5-[1,3]Dioxan-2-yl-2-methoxy-phenoxy)-phenyl]-ethyl}-phenoxy)-3-methoxy-benzoic acid methyl ester 
• 101554-02-3 diethyl <3-methoxy-4-<3-<2-<4-(2-methoxy-5-formylphenoxy)phenyl>ethyl>phenoxy>benzyl>phosphonate 
• 101554-00-1 diethyl <4-<2-methoxy-5-(1,3-dioxan-2-yl)phenoxy>benzyl>phosphonate 
• 85318-27-0 riccardin B 
• 111436-62-5 diethyl <4-(2-methoxy-5-formylphenoxy)benzyl>phosphonate 

Relevant articles and documents

Total synthesis of cavicularin and riccardin C: Addressing the synthesis of an arene that adopts a boat configuration

(Chemical Equation Presented) A transannular ring contraction induced by the addition of an aryl radical intermediate to a proximal arene facilitated the construction of the highly strained macrocyclic core of cavicularin (1). The precursor, an iodinated

SYNTHESIS AND STRUCTURE CONFIRMATION OF RICCARDIN B, A MACROCYCLIC BIS(BIBENZYL) FROM THE LIVERWORT, RICCARDIA MULTIFIDA

Riccardin B, a cytotoxic bis(bibenzyl) obtained from a liverwort was synthesized via an intramolecular Wittig-type reaction and the structure was established unequivocally.