1245824-49-0

Basic information

• Product Name: 4-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl N,N-diethylcarbamate
• Synonyms: 4-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl N,N-diethylcarbamate
• CAS NO: 1245824-49-0
• Molecular Weight: 395.306
• Mol File: 1245824-49-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl N,N-diethylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl N,N-diethylcarbamate(1245824-49-0)
• EPA Substance Registry System: 4-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl N,N-diethylcarbamate(1245824-49-0)

Safety Data

• Hazardous Substances Data: 1245824-49-0(Hazardous Substances Data)

Upstream product

• 117947-77-0 O-(1,1′-biphenyl)-4-yl N,N-diethylcarbamate 
• 25015-63-8 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane 

Relevant articles and documents

Directed ortho borylation of phenol derivatives catalyzed by a silica-supported iridium complex

The directed ortho borylation of phenol derivatives protected with an N,N-diethylcarbamoyl group was efficiently catalyzed by an immobilized monophosphine-Ir system, which was prepared in situ from [Ir(OMe)(cod)] 2 and a silica-supported, compact phosphine. The utility of the carbamoyloxy group as a leaving group for metal-catalyzed cross-coupling reactions was demonstrated by its utilization in the synthesis of a terphenyl derivative.