89936-29-8

Basic information

• Product Name: 2-(3,5-dibromo-4-methoxyphenyl)acetic acid
• Synonyms: 2-(3,5-dibromo-4-methoxyphenyl)acetic acid
• CAS NO: 89936-29-8
• Molecular Weight: 323.969
• Mol File: 89936-29-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(3,5-dibromo-4-methoxyphenyl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,5-dibromo-4-methoxyphenyl)acetic acid(89936-29-8)
• EPA Substance Registry System: 2-(3,5-dibromo-4-methoxyphenyl)acetic acid(89936-29-8)

Safety Data

• Hazardous Substances Data: 89936-29-8(Hazardous Substances Data)

Upstream product

• 23786-14-3 4-methoxy-phenyl acetic acid methyl ester 
• 14199-15-6 Methyl 4-hydroxyphenylacetate 
• 212688-03-4 3,5-dibromo-4-methoxy-phenyl acetic acid methyl ester 
• 104-01-8 4-Methoxyphenylacetic acid 
• 212688-02-3 3,5-dibromo-4-hydroxyphenylacetic acid methyl ester 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 1007893-78-8 (3,5-dibromo-4-hydroxyphenyl)(9H-pyrido[3,4-b]indol-1-yl)methanone 
• 1007893-79-9 (6-bromo-9H-pyrido[3,4-b]indol-1-yl)(3,5-dibromo-4-hydroxyphenyl)methanone 
• 1007893-80-2 (7-bromo-9H-pyrido[3,4-b]indol-1-yl)(3,5-dibromo-4-hydroxyphenyl)methanone 
• 1563242-87-4 2-(3,5-dibromo-4-methoxyphenyl)-N-(5-(dimethylamino)pentyl)acetamide 
• 74007-21-9 N-<2-(3-methoxyphenyl)ethyl>(3-hydroxy-4-methoxyphenyl)acetamide 

Relevant articles and documents

Synthesis of alkaloid pulmonarin B and its application in the prevention and control of plant viruses and mycosis

The present invention relates to the efficient synthesis of the alkaloid pulmonarin B and its application in the prevention and control of plant viruses and pathogenic diseases, the present invention is based on the systematic research literature, drawing

Total syntheses of eudistomins Y1-Y7 by an efficient one-pot process of tandem benzylic oxidation and aromatization of 1-benzyl-3,4-dihydro-β-carbolines

The first total synthesis of eudistomin Y7 (7) and total syntheses of eudistomins Y1-Y6 (1-6) are described. An efficient room-temperature conversion of 1-benzyl-3,4-dihydro-β-carbolines (11) into 1-benzoyl-β-carbolines (14) by a one-pot process of tandem benzylic oxidation and aromatization as the key step of these total syntheses was also studied in detail. The first total synthesis of eudistomin Y 7 (7) and total syntheses of eudistomins Y1-Y6 (1-6) are described. An efficient room-temperature conversion of 1-benzyl-3,4-dihydro-β-carbolines (11) into 1-benzoyl-β-carbolines (14) by a one-pot process of tandem benzylic oxidation and aromatization as the key step of these total syntheses was also studied in detail. Copyright

Preparation of Oxygenated Phenylacetic Acids

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