1258391-68-2

Basic information

• Product Name: (2,6-dibromo-3,5-dihydroxyphenyl)(3,5-dichloro-2-hydroxy-6-methoxy-4-methylphenyl)methanone
• Synonyms: (2,6-dibromo-3,5-dihydroxyphenyl)(3,5-dichloro-2-hydroxy-6-methoxy-4-methylphenyl)methanone
• CAS NO: 1258391-68-2
• Molecular Weight: 500.955
• Mol File: 1258391-68-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2,6-dibromo-3,5-dihydroxyphenyl)(3,5-dichloro-2-hydroxy-6-methoxy-4-methylphenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2,6-dibromo-3,5-dihydroxyphenyl)(3,5-dichloro-2-hydroxy-6-methoxy-4-methylphenyl)methanone(1258391-68-2)
• EPA Substance Registry System: (2,6-dibromo-3,5-dihydroxyphenyl)(3,5-dichloro-2-hydroxy-6-methoxy-4-methylphenyl)methanone(1258391-68-2)

Safety Data

• Hazardous Substances Data: 1258391-68-2(Hazardous Substances Data)

Upstream product

• 1258391-55-7 (2,6-dibromo-3,5-dimethoxyphenyl)(3,5-dichloro-2,6-dimethoxy-4-methylphenyl)-methanone 

Downstream Products

• 1258391-78-4 (2,6-dibromo-3,5-bis(methoxymethoxy)phenyl)(3,5-dichloro-2-hydroxy-6-methoxy-4-methylphenyl)methanone 

Relevant articles and documents

Total synthesis of the marine antibiotic pestalone and its surprisingly facile conversion into pestalalactone and pestalachloride A

Surprise, surprise! The total synthesis of the marine natural product pestalone (1), a highly substituted benzophenone with strong antibiotic acitivity, has provided insight into the surprising tendency of this and related molecules to undergo intramolecular Cannizzaro-Tishchenko-type reactions. Pestalone can be readily converted into pestalachloride A, a strongly antifungal metabolite isolated from an endophytic fungus, by simple treatment with ammonia at pH 8.