143592-82-9

Basic information

• Product Name: 3,4-Bis(benzyloxy)-5-brombenzaldehyd-diethylacetal
• Synonyms: 3,4-Bis(benzyloxy)-5-brombenzaldehyd-diethylacetal
• CAS NO: 143592-82-9
• Molecular Weight: 471.391
• Mol File: 143592-82-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,4-Bis(benzyloxy)-5-brombenzaldehyd-diethylacetal(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Bis(benzyloxy)-5-brombenzaldehyd-diethylacetal(143592-82-9)
• EPA Substance Registry System: 3,4-Bis(benzyloxy)-5-brombenzaldehyd-diethylacetal(143592-82-9)

Safety Data

• Hazardous Substances Data: 143592-82-9(Hazardous Substances Data)

Upstream product

• 124662-50-6 3,4-Bis(benzyloxy)-5-brombenzaldehyd 
• 122-51-0 orthoformic acid triethyl ester 

Downstream Products

• 143593-01-5 (E)-4',5-Bis(benzyloxy)-2'-<2-(3,4-bis(benzyloxy)-5-<4-(methoxycarbonyl)phenoxy>phenyl)ethenyl>-4-methoxybiphenyl-2-carbonsaeure-methylester 
• 143593-02-6 (Z)-4',5-Bis(benzyloxy)-2'-<2-(3,4-bis(benzyloxy)-5-<4-(methoxycarbonyl)phenoxy>phenyl)ethenyl>-4-methoxybiphenyl-2-carbonsaeure-methylester 
• 143617-60-1 (E)-4'-(Benzyloxy)-2'-<2-(3,4-bis(benzyloxy)-5-<4-(methoxycarbonyl)phenoxy>phenyl)ethenyl>-4-methoxybiphenyl-2-carbonsaeure-methylester 
• 143592-92-1 (Z)-4'-(Benzyloxy)-2'-<2-(3,4-bis(benzyloxy)-5-<4-(methoxycarbonyl)phenoxy>phenyl)ethenyl>-4-methoxybiphenyl-2-carbonsaeure-methylester 
• 143592-89-6 (3,4-Bis(benzyloxy)-5-<4-(methoxycarbonyl)phenoxy>benzyl)triphenylphosphonium-bromid 
• 143592-87-4 4-<2,3-Bis(benzyloxy)-5-(hydroxymethyl)phenoxy>benzoesaeure-methylester 
• 143592-88-5 4-<2,3-Bis(benzyloxy)-5-(brommethyl)phenoxy>benzoesaeure-methylester 
• 143592-86-3 4-<2,3-Bis(benzyloxy)-5-formylphenoxy>benzoesaeure-methylester 
• 143592-85-2 3,4-Bis(benzyloxy)-5-hydroxybenzaldehyd-diethylacetal 
• 143592-84-1 3,4-Bis(benzyloxy)-5-hydroxybenzaldehyd 

Relevant articles and documents

Synthesis of Plagiochins A and B, Macrocyclic Bis(bibenzyl) Ethers from Plagiochila acantophylla

Plagiochins A (1) and B (2), macrocyclic bis(bibenzyl) ethers with a 16-membered ring, are synthesized.The key steps are the Pd(0)-catalyzed C-C coupling of an areneboronic acid (18) with an aryl bromide with formation of a biphenyl (13), Ullmann ether sy