1325729-38-1

Basic information

• Product Name: (S)-(+)-4,4,5,5-tetramethyl-2-(2-(3-(trifluoromethyl)phenyl)propyl)-1,3,2-dioxaborolane
• Synonyms: (S)-(+)-4,4,5,5-tetramethyl-2-(2-(3-(trifluoromethyl)phenyl)propyl)-1,3,2-dioxaborolane
• CAS NO: 1325729-38-1
• Molecular Weight: 314.156
• Mol File: 1325729-38-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-(+)-4,4,5,5-tetramethyl-2-(2-(3-(trifluoromethyl)phenyl)propyl)-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-4,4,5,5-tetramethyl-2-(2-(3-(trifluoromethyl)phenyl)propyl)-1,3,2-dioxaborolane(1325729-38-1)
• EPA Substance Registry System: (S)-(+)-4,4,5,5-tetramethyl-2-(2-(3-(trifluoromethyl)phenyl)propyl)-1,3,2-dioxaborolane(1325729-38-1)

Safety Data

• Hazardous Substances Data: 1325729-38-1(Hazardous Substances Data)

Upstream product

• 368-79-6 2-<3-(Trifluoromethyl)phenyl>propene 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 
• 73183-34-3 bis(pinacol)diborane 

Relevant articles and documents

Iminopyridine oxazoline iron catalyst for asymmetric hydroboration of 1,1-disubtituted aryl alkenes

The highly regio- and enantioselective iron-catalyzed anti-Markovnikov hydroboration of 1,1-disubstituted aryl alkenes is reported by using a novel chiral iminopyridine oxazoline (IPO) ligand, in which the iminopyridine group is proposed to stabilize the iron and chiral oxazoline group to control enantioselectivity. This distinct class of reactive IPO ligands will likely be of high value for a large variety of asymmetric transformations using first-row transition metals.