1246431-54-8

Basic information

• Product Name: C₁₈H₁₅Cl₃O₆
• Synonyms: C₁₈H₁₅Cl₃O₆
• CAS NO: 1246431-54-8
• Molecular Weight: 433.673
• Mol File: 1246431-54-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₈H₁₅Cl₃O₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₈H₁₅Cl₃O₆(1246431-54-8)
• EPA Substance Registry System: C₁₈H₁₅Cl₃O₆(1246431-54-8)

Safety Data

• Hazardous Substances Data: 1246431-54-8(Hazardous Substances Data)

Upstream product

• 409366-27-4 (3,5-dichloro-4-hydroxyphenyl)acetic acid methyl ester 
• 14199-15-6 Methyl 4-hydroxyphenylacetate 
• 1246431-52-6 C₁₉H₁₇Cl₃O₇ 

Downstream Products

• 42583-41-5 2-{4-[5-(carboxymethyl)-2-methoxyphenoxy]phenyl}acetic acid 
• 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 
• 1246431-55-9 C₁₇H₁₃Cl₃O₆ 
• 5884-67-3 armepavine 
• 1934-93-6 6,7-dimethoxy-1-(4-methoxybenzyl)-2-methyl-1,2,3,4-tetrahydroisoquinoline 

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

Electrochemical construction of the diaryl ethers: A synthetic approach to o-methylthalibrine

Electrochemical dimerization of halogenated p-hydroxyphenylacetic acid derivatives followed by Zn reduction provided the corresponding diaryl ethers. Manipulation of the reduction step using several procedures increased its efficiency, which enabled the construction of o-methylthalibrine, an isoquinoline-class alkaloid.