42583-41-5

Basic information

• Product Name: 2-{4-[5-(carboxymethyl)-2-methoxyphenoxy]phenyl}acetic acid
• Synonyms: 2-{4-[5-(carboxymethyl)-2-methoxyphenoxy]phenyl}acetic acid
• CAS NO: 42583-41-5
• Molecular Weight: 316.31
• Mol File: 42583-41-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-{4-[5-(carboxymethyl)-2-methoxyphenoxy]phenyl}acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{4-[5-(carboxymethyl)-2-methoxyphenoxy]phenyl}acetic acid(42583-41-5)
• EPA Substance Registry System: 2-{4-[5-(carboxymethyl)-2-methoxyphenoxy]phenyl}acetic acid(42583-41-5)

Safety Data

• Hazardous Substances Data: 42583-41-5(Hazardous Substances Data)

Upstream product

• 854633-65-1 (4-methoxy-3,4'-oxy-diphenyl)-di-acetic acid diamide 
• 1246431-54-8 C₁₈H₁₅Cl₃O₆ 
• 1580442-44-9 methyl 2-{4-hydroxy-3-[4-(2-methoxy-2-oxoethyl)phenoxy]phenyl}acetate 
• 409366-27-4 (3,5-dichloro-4-hydroxyphenyl)acetic acid methyl ester 
• 1246431-52-6 C₁₉H₁₇Cl₃O₇ 
• 75208-24-1 4',5-dichloromethyl-2-methoxydiphenyl ether 
• 1695-04-1 2-methoxyphenyl phenyl ether 
• 38692-80-7 2-(3-bromo-4-hydroxyphenyl)acetic acid 
• 854166-24-8 4-methoxy-3,4'-oxy-di-benzoyl chloride 
• 24724-87-6 aristelegin-C 
• 14199-15-6 Methyl 4-hydroxyphenylacetate 
• 156-38-7 4-hydroxyphenylacetate 
• 857567-71-6 (5-diazoacetyl-2-methoxy-phenyl)-(4-diazoacetyl-phenyl)-ether 
• 857168-31-1 (4-methoxy-3,4'-oxy-diphenyl)-di-acetonitrile 

Downstream Products

• 59654-05-6 (+)-O-methylthalibrine 
• 14400-96-5 (S)-armepavine 
• 524-20-9 armepavine 
• 3423-02-7 (R)-(-)-O-methylarmepavine 
• 5701-00-8 (R)-O-methylarmepavine 
• 5884-67-3 armepavine 
• 1934-93-6 6,7-dimethoxy-1-(4-methoxybenzyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline 
• 5884-61-7 (4-hydroxy-3,4'-oxy-diphenyl)-di-acetic acid 

Relevant articles and documents

Synthesis of (+)-O-methylthalibrine by employing a stereocontrolled Bischler-Napieralski reaction and an electrochemically generated diaryl ether

An efficient electrochemical four-step route was developed for the preparation of diaryl ether derivatives by using halogenation and dehalogenation processes in addition to electrochemical phenolic oxidation and reduction reactions. The synthesis of (+)-O