657394-21-3

Basic information

• Product Name: Acetamide, N-2-propenyl-N-[4-(2-propenyloxy)phenyl]-
• CAS NO: 657394-21-3
• Molecular Formula: C14H17NO2
• Molecular Weight: 231.294
• Mol File: 657394-21-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Acetamide, N-2-propenyl-N-[4-(2-propenyloxy)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-2-propenyl-N-[4-(2-propenyloxy)phenyl]-(657394-21-3)
• EPA Substance Registry System: Acetamide, N-2-propenyl-N-[4-(2-propenyloxy)phenyl]-(657394-21-3)

Safety Data

• Hazardous Substances Data: 657394-21-3(Hazardous Substances Data)

Upstream product

• 6622-73-7 4-acetamidophenyl allyl ether 
• 106-95-6 allyl bromide 
• 103-90-2 4-acetaminophenol 
• 123-30-8 4-amino-phenol 
• 48121-05-7 4-Allylamino-phenol 
• 657394-20-2 acetic acid 4-(acetyl-allyl-amino)-phenyl ester 
• 103796-98-1 N-allyl-N-(4-hydroxyphenyl)acetamide 

Downstream Products

• 657394-02-0 allyl-(4-allyloxyphenyl)-N-ethylamine 
• 1688-69-3 p-allyloxyaniline 
• 103796-98-1 N-allyl-N-(4-hydroxyphenyl)acetamide 
• 103-90-2 4-acetaminophenol 
• 657394-05-3 allyl-(4-allyloxyphenyl)-amine 

Relevant articles and documents

Nickel-catalyzed deallylation of aryl allyl ethers with hydrosilanes

An efficient and mild catalytic deallylation method of aryl allyl ethers is developed, with commercially available Ni(COD)2 as catalyst precursor, simple substituted bipyridine as ligand and air-stable hydrosilanes. The process is compatible with a variety of functional groups and the desired phenol products can be obtained with excellent yields and selectivity. Besides, by detection or isolation of key intermediates, mechanism studies confirm that the deallylation undergoes η3-allylnickel intermediate pathway.