127502-55-0

Basic information

• Product Name: 2-Bromo-4,6-diisopropylphenol
• Synonyms: 2-Bromo-4,6-diisopropylphenol
• CAS NO: 127502-55-0
• Molecular Weight: 257.17
• Mol File: 127502-55-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Bromo-4,6-diisopropylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-4,6-diisopropylphenol(127502-55-0)
• EPA Substance Registry System: 2-Bromo-4,6-diisopropylphenol(127502-55-0)

Safety Data

• Hazardous Substances Data: 127502-55-0(Hazardous Substances Data)

Upstream product

• 2934-05-6 2,4-diisopropylphenol 
• 7439-89-6 iron 
• 2215-21-6 3,5-diisopropylsalicylic acid 

Downstream Products

• 127502-57-2 1-Benzyloxy-6-(p-fluorophenyl)-2,4-diisopropylbenzene 
• 127502-56-1 1-Benzyloxy-2-bromo-4,6-diisopropylbenzene 

Relevant articles and documents

3,5-di-iso-propyl-heptatrienoic acid derivatives having serum glucose reducing activity

Compounds of the formula where the variables have the meaning defined in the specification are capable of reducing serum glucose levels in diabetic mammals without the undesirable side effect of reducing serum thyroxine levels.

Arylation of Phenols. Convenient, Regiospecific Methods for Mono- or Bis-p-fluorophenylations, Suitable for Large Scale Syntheses

Phenols have been arylated by a palladium(0)-catalyzed coupling reaction.Two methods were used: a Grignard reagent of a protected phenol component 2 was coupled with a haloarene, or an umpolung (reversed reactivity) where unprotected phenolic halides 6 were coupled with aryl Grignard reagents.Bis-arylation and regiospecific ortho-, meta- and para-arylations were achieved.Aryl-aryl-couplings were insensitive to steric hindrance in the Grignard component, but were inhibited by sulfur-containing substituents in the phenolic component.A thiocyanate substituted biaryl was used to synthesize arylated phenols with various sulfur functionalities.