97571-08-9

Basic information

• Product Name: 2-(3,3-dimethyl-1-phenylbutan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• Synonyms: 2-(3,3-dimethyl-1-phenylbutan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• CAS NO: 97571-08-9
• Molecular Weight: 288.238
• Mol File: 97571-08-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(3,3-dimethyl-1-phenylbutan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3,3-dimethyl-1-phenylbutan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(97571-08-9)
• EPA Substance Registry System: 2-(3,3-dimethyl-1-phenylbutan-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane(97571-08-9)

Safety Data

• Hazardous Substances Data: 97571-08-9(Hazardous Substances Data)

Upstream product

• 99810-76-1 2-(tert-butyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 108-86-1 bromobenzene 
• 94242-82-7 2-(1-chloro-2-phenylethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Downstream Products

• 105735-62-4 3,3-dimethyl-1-phenyl-2-butanol 

Relevant articles and documents

Pd-Catalyzed Conjunctive Cross-Coupling between Grignard-Derived Boron “Ate” Complexes and C(sp2) Halides or Triflates: NaOTf as a Grignard Activator and Halide Scavenger

Catalytic enantioselective conjunctive cross-couplings that employ Grignard reagents are shown to furnish an array of nonracemic chiral organoboronic esters in an efficient and highly selective fashion. The utility of sodium triflate in facilitating this reaction is two-fold: it enables “ate” complex formation and overcomes catalytic inhibition by halide ions.