1007893-78-8

Basic information

• Product Name: (3,5-dibromo-4-hydroxyphenyl)(9H-pyrido[3,4-b]indol-1-yl)methanone
• Synonyms: (3,5-dibromo-4-hydroxyphenyl)(9H-pyrido[3,4-b]indol-1-yl)methanone
• CAS NO: 1007893-78-8
• Molecular Weight: 446.098
• Mol File: 1007893-78-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (3,5-dibromo-4-hydroxyphenyl)(9H-pyrido[3,4-b]indol-1-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (3,5-dibromo-4-hydroxyphenyl)(9H-pyrido[3,4-b]indol-1-yl)methanone(1007893-78-8)
• EPA Substance Registry System: (3,5-dibromo-4-hydroxyphenyl)(9H-pyrido[3,4-b]indol-1-yl)methanone(1007893-78-8)

Safety Data

• Hazardous Substances Data: 1007893-78-8(Hazardous Substances Data)

Upstream product

• 61-54-1 tryptamine 
• 2887-72-1 1-(3,5-dibromo-4-hydroxyphenyl)ethan-1-one 
• 74447-37-3 4-methylsulphonyloxyphenylacetaldehyde 
• 74447-38-4 4-(2-hydroxyethyl)phenyl methanesulfonate 
• 1007893-74-4 (4-hydroxyphenyl)(9H-pyrido[3,4-b]indol-1-yl)methanone 
• 1435263-15-2 4-(9H-pyrido[3,4-b]indole-1-carbonyl)phenyl methanesulfonate 
• 1435263-10-7 4-((2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-yl)methyl)phenyl methanesulfonate 
• 3156-51-2 3-[(E)-2-nitroeth-1-enyl]-1H-indole 
• 120-72-9 indole 
• 79324-79-1 1-(3,5-dibromo-4-methoxyphenyl)ethanone 
• 31731-23-4 3-(2-nitroethyl)indole 
• 89936-29-8 2-(3,5-dibromo-4-methoxyphenyl)acetic acid 
• 212688-03-4 3,5-dibromo-4-methoxy-phenyl acetic acid methyl ester 
• 104-01-8 4-Methoxyphenylacetic acid 

Downstream Products

• 1384431-87-1 eudistomin Y₁₀ 
• 1384431-85-9 eudistomin Y₈ 

Relevant articles and documents

A cascade coupling strategy for one-pot total synthesis of β-carboline and isoquinoline-containing natural products and derivatives

Multi-birds with one stone: A cascade coupling strategy was developed for the synthesis of β-carbolines. The method can direct the synthesis of β-carboline and isoquinoline-containing natural products with high yields. Moreover, this protocol can also be further applied towards the total synthesis of natural products fascaplysin and papaverin (see scheme). Copyright

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

Total synthesis of Eudistomins Y1-Y6

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