99321-88-7

Basic information

• Product Name: 4-phenoxy-2-phenylbut-2-en-1-ol
• Synonyms: 4-phenoxy-2-phenylbut-2-en-1-ol
• CAS NO: 99321-88-7
• Molecular Weight: 240.302
• Mol File: 99321-88-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-phenoxy-2-phenylbut-2-en-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenoxy-2-phenylbut-2-en-1-ol(99321-88-7)
• EPA Substance Registry System: 4-phenoxy-2-phenylbut-2-en-1-ol(99321-88-7)

Safety Data

• Hazardous Substances Data: 99321-88-7(Hazardous Substances Data)

Upstream product

• 97699-36-0 2-phenyl-2-vinyloxirane 
• 108-95-2 phenol 
• 1459246-62-8 4-phenyl-4-vinyl-1,3-dioxolan -2-one 

Relevant articles and documents

Palladium nano-particles as a recyclable catalyst for C-O bond formation under solvent free conditions

The development of green, economical and sustainable chemical processes is one of the primary challenges in organic chemistry. Herein, we report a recoverable heterogeneous palladium catalyst for the stereoselective synthesis of multi-functionalized allylic ethers under solvent free conditions. This method is based on in situ generated PdNP catalyzed O-allylation of alcohols with vinyl cyclic carbonates. Solvent-free conditions, easily recoverable catalysts, efficient recycling, and operational simplicity make the protocol green, economic and sustainable.

Pd-Catalyzed Enantio- and Regioselective Formation of Allylic Aryl Ethers

A general methodology for the synthesis of enantioenriched tertiary allylic aryl ethers through Pd-catalyzed decarboxylative reactions of vinyl cyclic carbonates and phenols is presented. Switching of the regioselectivity toward the formation of linear products by a judicious choice of the ligand is also reported.