910574-67-3

Basic information

• Product Name: tert-butyl(E)-3-([1,1′-biphenyl]-4-yl)acrylate
• Synonyms: tert-butyl(E)-3-([1,1′-biphenyl]-4-yl)acrylate
• CAS NO: 910574-67-3
• Molecular Weight: 280.367
• Mol File: 910574-67-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl(E)-3-([1,1′-biphenyl]-4-yl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl(E)-3-([1,1′-biphenyl]-4-yl)acrylate(910574-67-3)
• EPA Substance Registry System: tert-butyl(E)-3-([1,1′-biphenyl]-4-yl)acrylate(910574-67-3)

Safety Data

• Hazardous Substances Data: 910574-67-3(Hazardous Substances Data)

Upstream product

• 1663-39-4 tert-Butyl acrylate 
• 5122-99-6 4-iodophenylboronic acid 
• 98-80-6 phenylboronic acid 

Downstream Products

• 951174-33-7 tert-butyl (3S,αR)-3-(N-benzyl-N-α-methylbenzylamino)-3-(4-biphenyl)propanoate 
• 951174-25-7 tert-butyl (3R,αS)-3-(N-benzyl-N-α-methylbenzylamino)-3-(4-biphenyl)propanoate 
• 951174-48-4 (S)-3-amino-3-(4-biphenyl)propanoic acid 
• 951174-48-4 (R)-3-amino-3-(4-biphenyl)propanoic acid 

Relevant articles and documents

Chemoselective three-component coupling via a tandem Pd-catalyzed boron-Heck and Suzuki reactions

A new approach is herein reported to prepare biaryl derivatives via a tandem Pd-catalyzed boron-Heck and Suzuki reactions. This one-pot tandem process avoided purification or addition of extra catalyst between steps. The resulting biaryl compounds can be