151071-01-1

Basic information

• Product Name: 4-bromo-2-(3-methyl-2-butenyl)phenyl acetate
• Synonyms: 4-bromo-2-(3-methyl-2-butenyl)phenyl acetate
• CAS NO: 151071-01-1
• Molecular Weight: 283.165
• Mol File: 151071-01-1.mol

Chemical Properties

• CAS DataBase Reference: 4-bromo-2-(3-methyl-2-butenyl)phenyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-bromo-2-(3-methyl-2-butenyl)phenyl acetate(151071-01-1)
• EPA Substance Registry System: 4-bromo-2-(3-methyl-2-butenyl)phenyl acetate(151071-01-1)

Safety Data

• Hazardous Substances Data: 151071-01-1(Hazardous Substances Data)

Upstream product

• 870-63-3 prenyl bromide 
• 106-41-2 4-bromo-phenol 
• 75-36-5 acetyl chloride 
• 151071-00-0 4-bromo-2-(3-methylbut-2-en-1-yl)phenol 

Downstream Products

• 72704-01-9 (E)-methyl 3-[4-Hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]acrylate 
• 151071-02-2 methyl (E)-3-[4-(acetyloxy)-3-(3-methyl-2-butenyl)phenyl]-2-propenoate 

Relevant articles and documents

The synthesis of Plicatin B via the Heck reaction

The anti-microbial natural product Plicatin B has been synthesized in 53% overall yield using a Heck reaction as the key step. The optimum conditions for this reaction have been determined. Halophenols proved much less reactive than their corresponding ac

Synthesis of Phenolic Natural Products Using Palladium Catalyzed Coupling Reactions

Derivatives of 2,4-diiodophenol are shown to undergo palladium catalyzed carbonylation and alkyne coupling reactions in excellent to moderate yield and high regioselectivity.The scope of these reactions is explored.Palladium catalyzed reactions are employ