4974-86-1

Basic information

• Product Name: (+/-)-4-phenoxy-1-(1-hydroxy-propyl)-benzene
• Synonyms: (+/-)-4-phenoxy-1-(1-hydroxy-propyl)-benzene
• CAS NO: 4974-86-1
• Molecular Weight: 228.291
• Mol File: 4974-86-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (+/-)-4-phenoxy-1-(1-hydroxy-propyl)-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-4-phenoxy-1-(1-hydroxy-propyl)-benzene(4974-86-1)
• EPA Substance Registry System: (+/-)-4-phenoxy-1-(1-hydroxy-propyl)-benzene(4974-86-1)

Safety Data

• Hazardous Substances Data: 4974-86-1(Hazardous Substances Data)

Upstream product

• 67-36-7 4-phenoxy benzaldehyde 
• 925-90-6 ethylmagnesium bromide 
• 555-31-7 aluminum isopropoxide 

Downstream Products

• 103276-21-7 3,4-bis-(4-phenoxy-phenyl)-hexane 
• 4974-87-2 1-phenoxy-4-(prop-1-en-1-yl)benzene 
• 60319-66-6 1-phenoxy-4-(prop-1-en-1-yl)benzene 

Relevant articles and documents

Mechanistic aspects of aminium salt-catalyzed Diels-Alder reactions: The substrate ionization step

Substituent effects in the aminium salt catalyzed Diels-Alder reactions of 2,3-dimetnyl-1,3-butadiene with a series of meta and para substituted β-methylstyrenes are used to probe detailed mechanistic aspects of these reactions. Kinetic studies were carried out using two different aminium salt catalysts and also electrochemically, using anodic potentials corresponding to the oxidation potentials of the aminium salts. Substituent effects in the equilibrium oxidations of the styrene substrates to the corresponding cation radicals were also studied, via oxidation potential measurements. The results indicate rate determining one electron oxidation of the sytrenes to their cation radicals via an outer sphere electron transfer.